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University: University of Hong Kong

You searched for subject:(Synthesis). Showing records 1 – 30 of 229 total matches.

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University of Hong Kong

1. Xu, Ci. Towards synthesis of glycopeptides/glycoproteins via serine/threonine ligation.

Degree: PhD, 2015, University of Hong Kong

Glycoproteins are proteins that are post-translationally modified with oligosaccharides. Due to the non-template-mediated biosynthesis of glycoproteins in the nature, glycoproteins always exist as heterogeneous mixtures… (more)

Subjects/Keywords: Glycopeptides - Synthesis; Glycoproteins - Synthesis

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APA (6th Edition):

Xu, C. (2015). Towards synthesis of glycopeptides/glycoproteins via serine/threonine ligation. (Doctoral Dissertation). University of Hong Kong. Retrieved from Xu, C. [许辞]. (2015). Towards synthesis of glycopeptides/glycoproteins via serine/threonine ligation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5544001 ; http://hdl.handle.net/10722/212622

Chicago Manual of Style (16th Edition):

Xu, Ci. “Towards synthesis of glycopeptides/glycoproteins via serine/threonine ligation.” 2015. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Xu, C. [许辞]. (2015). Towards synthesis of glycopeptides/glycoproteins via serine/threonine ligation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5544001 ; http://hdl.handle.net/10722/212622.

MLA Handbook (7th Edition):

Xu, Ci. “Towards synthesis of glycopeptides/glycoproteins via serine/threonine ligation.” 2015. Web. 28 Mar 2020.

Vancouver:

Xu C. Towards synthesis of glycopeptides/glycoproteins via serine/threonine ligation. [Internet] [Doctoral dissertation]. University of Hong Kong; 2015. [cited 2020 Mar 28]. Available from: Xu, C. [许辞]. (2015). Towards synthesis of glycopeptides/glycoproteins via serine/threonine ligation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5544001 ; http://hdl.handle.net/10722/212622.

Council of Science Editors:

Xu C. Towards synthesis of glycopeptides/glycoproteins via serine/threonine ligation. [Doctoral Dissertation]. University of Hong Kong; 2015. Available from: Xu, C. [许辞]. (2015). Towards synthesis of glycopeptides/glycoproteins via serine/threonine ligation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5544001 ; http://hdl.handle.net/10722/212622


University of Hong Kong

2. Meng, Qi. Amine synthesis using tandem aza-witting/imine reduction reactions.

Degree: M. Phil., 2013, University of Hong Kong

Nowadays, both secondary and tertiary amines are playing vital roles in modern chemical industry as well as pharmaceutical industry. Various synthetic methods of amines have… (more)

Subjects/Keywords: Amines - Synthesis

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APA (6th Edition):

Meng, Q. (2013). Amine synthesis using tandem aza-witting/imine reduction reactions. (Masters Thesis). University of Hong Kong. Retrieved from Meng, Q. [孟琪]. (2013). Amine synthesis using tandem aza-witting/imine reduction reactions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177335 ; http://dx.doi.org/10.5353/th_b5177335 ; http://hdl.handle.net/10722/196452

Chicago Manual of Style (16th Edition):

Meng, Qi. “Amine synthesis using tandem aza-witting/imine reduction reactions.” 2013. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Meng, Q. [孟琪]. (2013). Amine synthesis using tandem aza-witting/imine reduction reactions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177335 ; http://dx.doi.org/10.5353/th_b5177335 ; http://hdl.handle.net/10722/196452.

MLA Handbook (7th Edition):

Meng, Qi. “Amine synthesis using tandem aza-witting/imine reduction reactions.” 2013. Web. 28 Mar 2020.

Vancouver:

Meng Q. Amine synthesis using tandem aza-witting/imine reduction reactions. [Internet] [Masters thesis]. University of Hong Kong; 2013. [cited 2020 Mar 28]. Available from: Meng, Q. [孟琪]. (2013). Amine synthesis using tandem aza-witting/imine reduction reactions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177335 ; http://dx.doi.org/10.5353/th_b5177335 ; http://hdl.handle.net/10722/196452.

Council of Science Editors:

Meng Q. Amine synthesis using tandem aza-witting/imine reduction reactions. [Masters Thesis]. University of Hong Kong; 2013. Available from: Meng, Q. [孟琪]. (2013). Amine synthesis using tandem aza-witting/imine reduction reactions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177335 ; http://dx.doi.org/10.5353/th_b5177335 ; http://hdl.handle.net/10722/196452


University of Hong Kong

3. 张银凤; Zhang, Yinfeng. Protein chemical synthesis by serine and threonine ligation.

Degree: PhD, 2014, University of Hong Kong

Landmark advances in the field of synthetic protein chemistry have enabled the preparation of complex, homogeneous proteins, including those that carry specific posttranslational modifications (PTMs).… (more)

Subjects/Keywords: Proteins - Synthesis

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APA (6th Edition):

张银凤; Zhang, Y. (2014). Protein chemical synthesis by serine and threonine ligation. (Doctoral Dissertation). University of Hong Kong. Retrieved from Zhang, Y. [张银凤]. (2014). Protein chemical synthesis by serine and threonine ligation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5295527 ; http://dx.doi.org/10.5353/th_b5295527 ; http://hdl.handle.net/10722/202359

Chicago Manual of Style (16th Edition):

张银凤; Zhang, Yinfeng. “Protein chemical synthesis by serine and threonine ligation.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Zhang, Y. [张银凤]. (2014). Protein chemical synthesis by serine and threonine ligation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5295527 ; http://dx.doi.org/10.5353/th_b5295527 ; http://hdl.handle.net/10722/202359.

MLA Handbook (7th Edition):

张银凤; Zhang, Yinfeng. “Protein chemical synthesis by serine and threonine ligation.” 2014. Web. 28 Mar 2020.

Vancouver:

张银凤; Zhang Y. Protein chemical synthesis by serine and threonine ligation. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2020 Mar 28]. Available from: Zhang, Y. [张银凤]. (2014). Protein chemical synthesis by serine and threonine ligation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5295527 ; http://dx.doi.org/10.5353/th_b5295527 ; http://hdl.handle.net/10722/202359.

Council of Science Editors:

张银凤; Zhang Y. Protein chemical synthesis by serine and threonine ligation. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Zhang, Y. [张银凤]. (2014). Protein chemical synthesis by serine and threonine ligation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5295527 ; http://dx.doi.org/10.5353/th_b5295527 ; http://hdl.handle.net/10722/202359


University of Hong Kong

4. Lam, Hiu-yung. Total synthesis of daptomycin and other cyclic peptides via Ser/Thr ligation-mediated peptide cyclization.

Degree: PhD, 2014, University of Hong Kong

Head-to-tail cyclic peptides with a wide range of ring sizes have been discovered in various organisms including bacteria, fungi, plants and animals. Many of them… (more)

Subjects/Keywords: Peptides - Synthesis

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APA (6th Edition):

Lam, H. (2014). Total synthesis of daptomycin and other cyclic peptides via Ser/Thr ligation-mediated peptide cyclization. (Doctoral Dissertation). University of Hong Kong. Retrieved from Lam, H. [林曉勇]. (2014). Total synthesis of daptomycin and other cyclic peptides via Ser/Thr ligation-mediated peptide cyclization. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334864 ; http://dx.doi.org/10.5353/th_b5334864 ; http://hdl.handle.net/10722/207198

Chicago Manual of Style (16th Edition):

Lam, Hiu-yung. “Total synthesis of daptomycin and other cyclic peptides via Ser/Thr ligation-mediated peptide cyclization.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Lam, H. [林曉勇]. (2014). Total synthesis of daptomycin and other cyclic peptides via Ser/Thr ligation-mediated peptide cyclization. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334864 ; http://dx.doi.org/10.5353/th_b5334864 ; http://hdl.handle.net/10722/207198.

MLA Handbook (7th Edition):

Lam, Hiu-yung. “Total synthesis of daptomycin and other cyclic peptides via Ser/Thr ligation-mediated peptide cyclization.” 2014. Web. 28 Mar 2020.

Vancouver:

Lam H. Total synthesis of daptomycin and other cyclic peptides via Ser/Thr ligation-mediated peptide cyclization. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2020 Mar 28]. Available from: Lam, H. [林曉勇]. (2014). Total synthesis of daptomycin and other cyclic peptides via Ser/Thr ligation-mediated peptide cyclization. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334864 ; http://dx.doi.org/10.5353/th_b5334864 ; http://hdl.handle.net/10722/207198.

Council of Science Editors:

Lam H. Total synthesis of daptomycin and other cyclic peptides via Ser/Thr ligation-mediated peptide cyclization. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Lam, H. [林曉勇]. (2014). Total synthesis of daptomycin and other cyclic peptides via Ser/Thr ligation-mediated peptide cyclization. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334864 ; http://dx.doi.org/10.5353/th_b5334864 ; http://hdl.handle.net/10722/207198


University of Hong Kong

5. 梁宇律; Leung, Yu-lut. Design, synthesis and functionalization of luminescent alkynylplatinum(II) complexes of tridentate N-donor ligands as building blocks for metallofoldamers, supramolecular assemblies and nanostructures.

Degree: PhD, 2013, University of Hong Kong

Li Ka Shing Prize, The Best PhD Thesis in the Faculties of Dentistry, Engineering, Medicine and Science (University of Hong Kong), 2012-2013.

published_or_final_version

Chemistry

Doctoral

Doctor of Philosophy

Subjects/Keywords: Platinum compounds - Synthesis; Complex compounds - Synthesis

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APA (6th Edition):

梁宇律; Leung, Y. (2013). Design, synthesis and functionalization of luminescent alkynylplatinum(II) complexes of tridentate N-donor ligands as building blocks for metallofoldamers, supramolecular assemblies and nanostructures. (Doctoral Dissertation). University of Hong Kong. Retrieved from Leung, Y. [梁宇律]. (2013). Design, synthesis and functionalization of luminescent alkynylplatinum(II) complexes of tridentate N-donor ligands as building blocks for metallofoldamers, supramolecular assemblies and nanostructures. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719452 ; http://hdl.handle.net/10722/223579

Chicago Manual of Style (16th Edition):

梁宇律; Leung, Yu-lut. “Design, synthesis and functionalization of luminescent alkynylplatinum(II) complexes of tridentate N-donor ligands as building blocks for metallofoldamers, supramolecular assemblies and nanostructures.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Leung, Y. [梁宇律]. (2013). Design, synthesis and functionalization of luminescent alkynylplatinum(II) complexes of tridentate N-donor ligands as building blocks for metallofoldamers, supramolecular assemblies and nanostructures. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719452 ; http://hdl.handle.net/10722/223579.

MLA Handbook (7th Edition):

梁宇律; Leung, Yu-lut. “Design, synthesis and functionalization of luminescent alkynylplatinum(II) complexes of tridentate N-donor ligands as building blocks for metallofoldamers, supramolecular assemblies and nanostructures.” 2013. Web. 28 Mar 2020.

Vancouver:

梁宇律; Leung Y. Design, synthesis and functionalization of luminescent alkynylplatinum(II) complexes of tridentate N-donor ligands as building blocks for metallofoldamers, supramolecular assemblies and nanostructures. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2020 Mar 28]. Available from: Leung, Y. [梁宇律]. (2013). Design, synthesis and functionalization of luminescent alkynylplatinum(II) complexes of tridentate N-donor ligands as building blocks for metallofoldamers, supramolecular assemblies and nanostructures. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719452 ; http://hdl.handle.net/10722/223579.

Council of Science Editors:

梁宇律; Leung Y. Design, synthesis and functionalization of luminescent alkynylplatinum(II) complexes of tridentate N-donor ligands as building blocks for metallofoldamers, supramolecular assemblies and nanostructures. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Leung, Y. [梁宇律]. (2013). Design, synthesis and functionalization of luminescent alkynylplatinum(II) complexes of tridentate N-donor ligands as building blocks for metallofoldamers, supramolecular assemblies and nanostructures. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719452 ; http://hdl.handle.net/10722/223579


University of Hong Kong

6. 潘俊廷; Poon, Chun-ting. Design and synthesis of boron (III)-containing dithienylethenes – from multi-addressable and gated photochromism to photoswitchable luminescence functions.

Degree: PhD, 2012, University of Hong Kong

 A series of photochromic dithienylethene-containing triarylboranes has been synthesized and characterized. The X-ray crystal structure of (4,5-bis(2,5-dimethylthiophen-3-yl)-thiophen-2-yl)dimesitylborane has been determined. An intense electronic absorption band… (more)

Subjects/Keywords: Boron compounds - Synthesis; Photochromism; Ethylene compounds - Synthesis

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APA (6th Edition):

潘俊廷; Poon, C. (2012). Design and synthesis of boron (III)-containing dithienylethenes – from multi-addressable and gated photochromism to photoswitchable luminescence functions. (Doctoral Dissertation). University of Hong Kong. Retrieved from Poon, C. [潘俊廷]. (2012). Design and synthesis of boron (III)-containing dithienylethenes – from multi-addressable and gated photochromism to photoswitchable luminescence functions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4723401 ; http://dx.doi.org/10.5353/th_b4723401 ; http://hdl.handle.net/10722/207983

Chicago Manual of Style (16th Edition):

潘俊廷; Poon, Chun-ting. “Design and synthesis of boron (III)-containing dithienylethenes – from multi-addressable and gated photochromism to photoswitchable luminescence functions.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Poon, C. [潘俊廷]. (2012). Design and synthesis of boron (III)-containing dithienylethenes – from multi-addressable and gated photochromism to photoswitchable luminescence functions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4723401 ; http://dx.doi.org/10.5353/th_b4723401 ; http://hdl.handle.net/10722/207983.

MLA Handbook (7th Edition):

潘俊廷; Poon, Chun-ting. “Design and synthesis of boron (III)-containing dithienylethenes – from multi-addressable and gated photochromism to photoswitchable luminescence functions.” 2012. Web. 28 Mar 2020.

Vancouver:

潘俊廷; Poon C. Design and synthesis of boron (III)-containing dithienylethenes – from multi-addressable and gated photochromism to photoswitchable luminescence functions. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Poon, C. [潘俊廷]. (2012). Design and synthesis of boron (III)-containing dithienylethenes – from multi-addressable and gated photochromism to photoswitchable luminescence functions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4723401 ; http://dx.doi.org/10.5353/th_b4723401 ; http://hdl.handle.net/10722/207983.

Council of Science Editors:

潘俊廷; Poon C. Design and synthesis of boron (III)-containing dithienylethenes – from multi-addressable and gated photochromism to photoswitchable luminescence functions. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Poon, C. [潘俊廷]. (2012). Design and synthesis of boron (III)-containing dithienylethenes – from multi-addressable and gated photochromism to photoswitchable luminescence functions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4723401 ; http://dx.doi.org/10.5353/th_b4723401 ; http://hdl.handle.net/10722/207983


University of Hong Kong

7. Kwok, Chi-ho. Design and synthesis of functionalized alkynylplatinum (II) polypyridyl complexes and oligothienylenevinylene derivatives : from dye-sensitized solar cells to bilayer heterojunction photovoltaics.

Degree: PhD, 2012, University of Hong Kong

 A series of alkynylplatinum(II) polypyridine complexes with 4,4′,4′′-tricarboxy-2,2′:6′,2′′-terpyridine and 4,4′-dicarboxy-2,2′-bipyridine as TiO2 anchoring functionalities, has been successfully synthesized. Their photophysical, electrochemical and luminescence properties have… (more)

Subjects/Keywords: Photochemistry; Complex compounds - Synthesis; Platinum compounds - Synthesis

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APA (6th Edition):

Kwok, C. (2012). Design and synthesis of functionalized alkynylplatinum (II) polypyridyl complexes and oligothienylenevinylene derivatives : from dye-sensitized solar cells to bilayer heterojunction photovoltaics. (Doctoral Dissertation). University of Hong Kong. Retrieved from Kwok, C. [郭志豪]. (2012). Design and synthesis of functionalized alkynylplatinum (II) polypyridyl complexes and oligothienylenevinylene derivatives : from dye-sensitized solar cells to bilayer heterojunction photovoltaics. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4775269 ; http://dx.doi.org/10.5353/th_b4775269 ; http://hdl.handle.net/10722/208172

Chicago Manual of Style (16th Edition):

Kwok, Chi-ho. “Design and synthesis of functionalized alkynylplatinum (II) polypyridyl complexes and oligothienylenevinylene derivatives : from dye-sensitized solar cells to bilayer heterojunction photovoltaics.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Kwok, C. [郭志豪]. (2012). Design and synthesis of functionalized alkynylplatinum (II) polypyridyl complexes and oligothienylenevinylene derivatives : from dye-sensitized solar cells to bilayer heterojunction photovoltaics. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4775269 ; http://dx.doi.org/10.5353/th_b4775269 ; http://hdl.handle.net/10722/208172.

MLA Handbook (7th Edition):

Kwok, Chi-ho. “Design and synthesis of functionalized alkynylplatinum (II) polypyridyl complexes and oligothienylenevinylene derivatives : from dye-sensitized solar cells to bilayer heterojunction photovoltaics.” 2012. Web. 28 Mar 2020.

Vancouver:

Kwok C. Design and synthesis of functionalized alkynylplatinum (II) polypyridyl complexes and oligothienylenevinylene derivatives : from dye-sensitized solar cells to bilayer heterojunction photovoltaics. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Kwok, C. [郭志豪]. (2012). Design and synthesis of functionalized alkynylplatinum (II) polypyridyl complexes and oligothienylenevinylene derivatives : from dye-sensitized solar cells to bilayer heterojunction photovoltaics. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4775269 ; http://dx.doi.org/10.5353/th_b4775269 ; http://hdl.handle.net/10722/208172.

Council of Science Editors:

Kwok C. Design and synthesis of functionalized alkynylplatinum (II) polypyridyl complexes and oligothienylenevinylene derivatives : from dye-sensitized solar cells to bilayer heterojunction photovoltaics. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Kwok, C. [郭志豪]. (2012). Design and synthesis of functionalized alkynylplatinum (II) polypyridyl complexes and oligothienylenevinylene derivatives : from dye-sensitized solar cells to bilayer heterojunction photovoltaics. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4775269 ; http://dx.doi.org/10.5353/th_b4775269 ; http://hdl.handle.net/10722/208172


University of Hong Kong

8. Ou, Jun. Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters.

Degree: PhD, 2011, University of Hong Kong

 Two syntheses of non-cross-linked polystyrene-supported TADDOL-based phosphoric acid organocatalyst have been developed. The optimal polymer-supported catalyst 2.29d exhibited comparable catalytic activity to its small molecule… (more)

Subjects/Keywords: Asymmetric synthesis.; Catalysis.; Organic compounds - Synthesis.

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APA (6th Edition):

Ou, J. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters. (Doctoral Dissertation). University of Hong Kong. Retrieved from Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528

Chicago Manual of Style (16th Edition):

Ou, Jun. “Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters.” 2011. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528.

MLA Handbook (7th Edition):

Ou, Jun. “Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters.” 2011. Web. 28 Mar 2020.

Vancouver:

Ou J. Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters. [Internet] [Doctoral dissertation]. University of Hong Kong; 2011. [cited 2020 Mar 28]. Available from: Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528.

Council of Science Editors:

Ou J. Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters. [Doctoral Dissertation]. University of Hong Kong; 2011. Available from: Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528


University of Hong Kong

9. 曾家懿; Tsang, Ka-yi. Two dimensional transition metal dichalcogenides grown by chemical vapor deposition.

Degree: M. Phil., 2014, University of Hong Kong

An atomically thin film of semiconducting transition metal dichalcogenides (TMDCs) is emerging as a class of key materials in chemistry and physics due to their… (more)

Subjects/Keywords: Transition metal compounds - Synthesis; Chalcogenides - Synthesis

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APA (6th Edition):

曾家懿; Tsang, K. (2014). Two dimensional transition metal dichalcogenides grown by chemical vapor deposition. (Masters Thesis). University of Hong Kong. Retrieved from Tsang, K. [曾家懿]. (2014). Two dimensional transition metal dichalcogenides grown by chemical vapor deposition. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5544026 ; http://hdl.handle.net/10722/212604

Chicago Manual of Style (16th Edition):

曾家懿; Tsang, Ka-yi. “Two dimensional transition metal dichalcogenides grown by chemical vapor deposition.” 2014. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Tsang, K. [曾家懿]. (2014). Two dimensional transition metal dichalcogenides grown by chemical vapor deposition. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5544026 ; http://hdl.handle.net/10722/212604.

MLA Handbook (7th Edition):

曾家懿; Tsang, Ka-yi. “Two dimensional transition metal dichalcogenides grown by chemical vapor deposition.” 2014. Web. 28 Mar 2020.

Vancouver:

曾家懿; Tsang K. Two dimensional transition metal dichalcogenides grown by chemical vapor deposition. [Internet] [Masters thesis]. University of Hong Kong; 2014. [cited 2020 Mar 28]. Available from: Tsang, K. [曾家懿]. (2014). Two dimensional transition metal dichalcogenides grown by chemical vapor deposition. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5544026 ; http://hdl.handle.net/10722/212604.

Council of Science Editors:

曾家懿; Tsang K. Two dimensional transition metal dichalcogenides grown by chemical vapor deposition. [Masters Thesis]. University of Hong Kong; 2014. Available from: Tsang, K. [曾家懿]. (2014). Two dimensional transition metal dichalcogenides grown by chemical vapor deposition. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5544026 ; http://hdl.handle.net/10722/212604


University of Hong Kong

10. Lam, Ho-chuen. Design, synthesis and host-guest chemistry of rhodamine derivatives and their transition metal complexes.

Degree: M. Phil., 2012, University of Hong Kong

New classes of luminescent transition metal complexes, including the systems of rhenium(I) tricarbonyl diimine, cyclometalated iridium(III) diimine, cyclometalated rhodium(III) diimine, ruthenium(II) diimine and ruthenium(II) terpyridine… (more)

Subjects/Keywords: Rhodium compounds - Synthesis; Transition metal complexes - Synthesis

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APA (6th Edition):

Lam, H. (2012). Design, synthesis and host-guest chemistry of rhodamine derivatives and their transition metal complexes. (Masters Thesis). University of Hong Kong. Retrieved from Lam, H. [林浩銓]. (2012). Design, synthesis and host-guest chemistry of rhodamine derivatives and their transition metal complexes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5060562 ; http://dx.doi.org/10.5353/th_b5060562 ; http://hdl.handle.net/10722/198806

Chicago Manual of Style (16th Edition):

Lam, Ho-chuen. “Design, synthesis and host-guest chemistry of rhodamine derivatives and their transition metal complexes.” 2012. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Lam, H. [林浩銓]. (2012). Design, synthesis and host-guest chemistry of rhodamine derivatives and their transition metal complexes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5060562 ; http://dx.doi.org/10.5353/th_b5060562 ; http://hdl.handle.net/10722/198806.

MLA Handbook (7th Edition):

Lam, Ho-chuen. “Design, synthesis and host-guest chemistry of rhodamine derivatives and their transition metal complexes.” 2012. Web. 28 Mar 2020.

Vancouver:

Lam H. Design, synthesis and host-guest chemistry of rhodamine derivatives and their transition metal complexes. [Internet] [Masters thesis]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Lam, H. [林浩銓]. (2012). Design, synthesis and host-guest chemistry of rhodamine derivatives and their transition metal complexes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5060562 ; http://dx.doi.org/10.5353/th_b5060562 ; http://hdl.handle.net/10722/198806.

Council of Science Editors:

Lam H. Design, synthesis and host-guest chemistry of rhodamine derivatives and their transition metal complexes. [Masters Thesis]. University of Hong Kong; 2012. Available from: Lam, H. [林浩銓]. (2012). Design, synthesis and host-guest chemistry of rhodamine derivatives and their transition metal complexes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5060562 ; http://dx.doi.org/10.5353/th_b5060562 ; http://hdl.handle.net/10722/198806


University of Hong Kong

11. Hermeke, Julia. Chiral phosphonium ion tagged and spiroindane-based organocatalysts.

Degree: M. Phil., 2011, University of Hong Kong

The research on asymmetric organocatalysis has been intensifying since the beginning of 2000. The growing interest in this research area is driven by the importance… (more)

Subjects/Keywords: Organic compounds - Synthesis; Asymmetric synthesis; Catalysis

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APA (6th Edition):

Hermeke, J. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Masters Thesis). University of Hong Kong. Retrieved from Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871

Chicago Manual of Style (16th Edition):

Hermeke, Julia. “Chiral phosphonium ion tagged and spiroindane-based organocatalysts.” 2011. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871.

MLA Handbook (7th Edition):

Hermeke, Julia. “Chiral phosphonium ion tagged and spiroindane-based organocatalysts.” 2011. Web. 28 Mar 2020.

Vancouver:

Hermeke J. Chiral phosphonium ion tagged and spiroindane-based organocatalysts. [Internet] [Masters thesis]. University of Hong Kong; 2011. [cited 2020 Mar 28]. Available from: Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871.

Council of Science Editors:

Hermeke J. Chiral phosphonium ion tagged and spiroindane-based organocatalysts. [Masters Thesis]. University of Hong Kong; 2011. Available from: Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871


University of Hong Kong

12. 汪子玉; Wang, Ziyu. Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes.

Degree: PhD, 2012, University of Hong Kong

The synthesis of useful chiral skeletons from simple achiral starting materials is always the dream of organic chemists. In the past decades, organocatalysis has been… (more)

Subjects/Keywords: Nitroalkenes; Asymmetric synthesis; Dibenzofurans; Organic compounds - Synthesis

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APA (6th Edition):

汪子玉; Wang, Z. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388

Chicago Manual of Style (16th Edition):

汪子玉; Wang, Ziyu. “Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388.

MLA Handbook (7th Edition):

汪子玉; Wang, Ziyu. “Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes.” 2012. Web. 28 Mar 2020.

Vancouver:

汪子玉; Wang Z. Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388.

Council of Science Editors:

汪子玉; Wang Z. Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388


University of Hong Kong

13. He, Jiayun. Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine.

Degree: PhD, 2017, University of Hong Kong

The intramolecular (4+3) cycloadditions of epoxy enolsilane substrates 1.89 generated polycyclic cycloadducts 1.90 having bicyclo[5.3.0]decane frameworks, a skeleton which is common among terpenoid natural products… (more)

Subjects/Keywords: Organic compounds - Synthesis

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APA (6th Edition):

He, J. (2017). Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/241419

Chicago Manual of Style (16th Edition):

He, Jiayun. “Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine.” 2017. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. http://hdl.handle.net/10722/241419.

MLA Handbook (7th Edition):

He, Jiayun. “Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine.” 2017. Web. 28 Mar 2020.

Vancouver:

He J. Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine. [Internet] [Doctoral dissertation]. University of Hong Kong; 2017. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10722/241419.

Council of Science Editors:

He J. Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine. [Doctoral Dissertation]. University of Hong Kong; 2017. Available from: http://hdl.handle.net/10722/241419


University of Hong Kong

14. Xu, Shaobo. Studies towards syntheses of kainic acid.

Degree: PhD, 2012, University of Hong Kong

Kainoid amino acids are a family of none proteinogenic pyrrolidine dicarboxylic acids with similar structures and can be viewed as conformationally restricted analogues of the… (more)

Subjects/Keywords: Kainic acid - Synthesis.

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APA (6th Edition):

Xu, S. (2012). Studies towards syntheses of kainic acid. (Doctoral Dissertation). University of Hong Kong. Retrieved from Xu, S. [许少波]. (2012). Studies towards syntheses of kainic acid. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979941 ; http://dx.doi.org/10.5353/th_b4979941 ; http://hdl.handle.net/10722/181508

Chicago Manual of Style (16th Edition):

Xu, Shaobo. “Studies towards syntheses of kainic acid.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Xu, S. [许少波]. (2012). Studies towards syntheses of kainic acid. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979941 ; http://dx.doi.org/10.5353/th_b4979941 ; http://hdl.handle.net/10722/181508.

MLA Handbook (7th Edition):

Xu, Shaobo. “Studies towards syntheses of kainic acid.” 2012. Web. 28 Mar 2020.

Vancouver:

Xu S. Studies towards syntheses of kainic acid. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Xu, S. [许少波]. (2012). Studies towards syntheses of kainic acid. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979941 ; http://dx.doi.org/10.5353/th_b4979941 ; http://hdl.handle.net/10722/181508.

Council of Science Editors:

Xu S. Studies towards syntheses of kainic acid. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Xu, S. [许少波]. (2012). Studies towards syntheses of kainic acid. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979941 ; http://dx.doi.org/10.5353/th_b4979941 ; http://hdl.handle.net/10722/181508


University of Hong Kong

15. Hung, Faan-fung. Luminescent platinum(II), palladium(II) and gold(III) complexes containing isocyanide, alkynyl and N-heterocyclic carbene ligands : synthesis, photophysical properties and material applications.

Degree: PhD, 2014, University of Hong Kong

 Several cyclometalated Pt(II) isocyanide complexes containing C-deprotonated C^N^C ligands (C^N^C = 2,6-diphenylpyridine derivatives) were synthesized. These complexes display orange-red emissions with max at 582–619 nm… (more)

Subjects/Keywords: Organogold compounds - Synthesis; Organopalladium compounds - Synthesis; Organoplatinum compounds - Synthesis

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APA (6th Edition):

Hung, F. (2014). Luminescent platinum(II), palladium(II) and gold(III) complexes containing isocyanide, alkynyl and N-heterocyclic carbene ligands : synthesis, photophysical properties and material applications. (Doctoral Dissertation). University of Hong Kong. Retrieved from Hung, F. [孔繁峰]. (2014). Luminescent platinum(II), palladium(II) and gold(III) complexes containing isocyanide, alkynyl and N-heterocyclic carbene ligands : synthesis, photophysical properties and material applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5312313 ; http://dx.doi.org/10.5353/th_b5312313 ; http://hdl.handle.net/10722/219337

Chicago Manual of Style (16th Edition):

Hung, Faan-fung. “Luminescent platinum(II), palladium(II) and gold(III) complexes containing isocyanide, alkynyl and N-heterocyclic carbene ligands : synthesis, photophysical properties and material applications.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Hung, F. [孔繁峰]. (2014). Luminescent platinum(II), palladium(II) and gold(III) complexes containing isocyanide, alkynyl and N-heterocyclic carbene ligands : synthesis, photophysical properties and material applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5312313 ; http://dx.doi.org/10.5353/th_b5312313 ; http://hdl.handle.net/10722/219337.

MLA Handbook (7th Edition):

Hung, Faan-fung. “Luminescent platinum(II), palladium(II) and gold(III) complexes containing isocyanide, alkynyl and N-heterocyclic carbene ligands : synthesis, photophysical properties and material applications.” 2014. Web. 28 Mar 2020.

Vancouver:

Hung F. Luminescent platinum(II), palladium(II) and gold(III) complexes containing isocyanide, alkynyl and N-heterocyclic carbene ligands : synthesis, photophysical properties and material applications. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2020 Mar 28]. Available from: Hung, F. [孔繁峰]. (2014). Luminescent platinum(II), palladium(II) and gold(III) complexes containing isocyanide, alkynyl and N-heterocyclic carbene ligands : synthesis, photophysical properties and material applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5312313 ; http://dx.doi.org/10.5353/th_b5312313 ; http://hdl.handle.net/10722/219337.

Council of Science Editors:

Hung F. Luminescent platinum(II), palladium(II) and gold(III) complexes containing isocyanide, alkynyl and N-heterocyclic carbene ligands : synthesis, photophysical properties and material applications. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Hung, F. [孔繁峰]. (2014). Luminescent platinum(II), palladium(II) and gold(III) complexes containing isocyanide, alkynyl and N-heterocyclic carbene ligands : synthesis, photophysical properties and material applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5312313 ; http://dx.doi.org/10.5353/th_b5312313 ; http://hdl.handle.net/10722/219337


University of Hong Kong

16. 洪鹏达.; Hong, Pengda. Synthesis and characterization of LiNi0.6Mn0.35Co0.05O2 and Li2FeSiO4/C as electrodes for rechargeable lithium ion battery.

Degree: M. Phil., 2011, University of Hong Kong

The rechargeable lithium ion batteries (LIB) are playing increasingly important roles in powering portal commercial electronic devices. They are also the potential power sources of… (more)

Subjects/Keywords: Cobalt compounds - Synthesis.; Lithium compounds - Synthesis.; Cathodes.; Lithium ion batteries.; Silicon compounds - Synthesis.; Iron compounds - Synthesis.; Manganese compounds - Synthesis.

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APA (6th Edition):

洪鹏达.; Hong, P. (2011). Synthesis and characterization of LiNi0.6Mn0.35Co0.05O2 and Li2FeSiO4/C as electrodes for rechargeable lithium ion battery. (Masters Thesis). University of Hong Kong. Retrieved from Hong, P. [洪鹏达]. (2011). Synthesis and characterization of LiNi0.6Mn0.35Co0.05O2 and Li2FeSiO4/C as electrodes for rechargeable lithium ion battery. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4715029 ; http://dx.doi.org/10.5353/th_b4715029 ; http://hdl.handle.net/10722/179879

Chicago Manual of Style (16th Edition):

洪鹏达.; Hong, Pengda. “Synthesis and characterization of LiNi0.6Mn0.35Co0.05O2 and Li2FeSiO4/C as electrodes for rechargeable lithium ion battery.” 2011. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Hong, P. [洪鹏达]. (2011). Synthesis and characterization of LiNi0.6Mn0.35Co0.05O2 and Li2FeSiO4/C as electrodes for rechargeable lithium ion battery. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4715029 ; http://dx.doi.org/10.5353/th_b4715029 ; http://hdl.handle.net/10722/179879.

MLA Handbook (7th Edition):

洪鹏达.; Hong, Pengda. “Synthesis and characterization of LiNi0.6Mn0.35Co0.05O2 and Li2FeSiO4/C as electrodes for rechargeable lithium ion battery.” 2011. Web. 28 Mar 2020.

Vancouver:

洪鹏达.; Hong P. Synthesis and characterization of LiNi0.6Mn0.35Co0.05O2 and Li2FeSiO4/C as electrodes for rechargeable lithium ion battery. [Internet] [Masters thesis]. University of Hong Kong; 2011. [cited 2020 Mar 28]. Available from: Hong, P. [洪鹏达]. (2011). Synthesis and characterization of LiNi0.6Mn0.35Co0.05O2 and Li2FeSiO4/C as electrodes for rechargeable lithium ion battery. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4715029 ; http://dx.doi.org/10.5353/th_b4715029 ; http://hdl.handle.net/10722/179879.

Council of Science Editors:

洪鹏达.; Hong P. Synthesis and characterization of LiNi0.6Mn0.35Co0.05O2 and Li2FeSiO4/C as electrodes for rechargeable lithium ion battery. [Masters Thesis]. University of Hong Kong; 2011. Available from: Hong, P. [洪鹏达]. (2011). Synthesis and characterization of LiNi0.6Mn0.35Co0.05O2 and Li2FeSiO4/C as electrodes for rechargeable lithium ion battery. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4715029 ; http://dx.doi.org/10.5353/th_b4715029 ; http://hdl.handle.net/10722/179879


University of Hong Kong

17. Yu, Yang. Synthetic studies towards (+)-anthecularin.

Degree: PhD, 2015, University of Hong Kong

published_or_final_version

Chemistry

Doctoral

Doctor of Philosophy

Subjects/Keywords: Lactones - Synthesis

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APA (6th Edition):

Yu, Y. (2015). Synthetic studies towards (+)-anthecularin. (Doctoral Dissertation). University of Hong Kong. Retrieved from Yu, Y. [于洋]. (2015). Synthetic studies towards (+)-anthecularin. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5760953 ; http://hdl.handle.net/10722/226790

Chicago Manual of Style (16th Edition):

Yu, Yang. “Synthetic studies towards (+)-anthecularin.” 2015. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Yu, Y. [于洋]. (2015). Synthetic studies towards (+)-anthecularin. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5760953 ; http://hdl.handle.net/10722/226790.

MLA Handbook (7th Edition):

Yu, Yang. “Synthetic studies towards (+)-anthecularin.” 2015. Web. 28 Mar 2020.

Vancouver:

Yu Y. Synthetic studies towards (+)-anthecularin. [Internet] [Doctoral dissertation]. University of Hong Kong; 2015. [cited 2020 Mar 28]. Available from: Yu, Y. [于洋]. (2015). Synthetic studies towards (+)-anthecularin. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5760953 ; http://hdl.handle.net/10722/226790.

Council of Science Editors:

Yu Y. Synthetic studies towards (+)-anthecularin. [Doctoral Dissertation]. University of Hong Kong; 2015. Available from: Yu, Y. [于洋]. (2015). Synthetic studies towards (+)-anthecularin. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5760953 ; http://hdl.handle.net/10722/226790


University of Hong Kong

18. Zhao, Tianqi. Catalytic formation of polycyclic aromatic hydrocarbons from acetylene over silicon carbide.

Degree: M. Phil., 2014, University of Hong Kong

In this research, silicon carbide (SiC) has been confirmed to be catalytically active for the formation of polycyclic aromatic hydrocarbons (PAHs) from acetylene (C2H2). Aromatization… (more)

Subjects/Keywords: Silicon carbide; Acetylene; Hydrocarbons - Synthesis

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APA (6th Edition):

Zhao, T. (2014). Catalytic formation of polycyclic aromatic hydrocarbons from acetylene over silicon carbide. (Masters Thesis). University of Hong Kong. Retrieved from Zhao, T. [趙天騏]. (2014). Catalytic formation of polycyclic aromatic hydrocarbons from acetylene over silicon carbide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5388030 ; http://dx.doi.org/10.5353/th_b5388030 ; http://hdl.handle.net/10722/208605

Chicago Manual of Style (16th Edition):

Zhao, Tianqi. “Catalytic formation of polycyclic aromatic hydrocarbons from acetylene over silicon carbide.” 2014. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Zhao, T. [趙天騏]. (2014). Catalytic formation of polycyclic aromatic hydrocarbons from acetylene over silicon carbide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5388030 ; http://dx.doi.org/10.5353/th_b5388030 ; http://hdl.handle.net/10722/208605.

MLA Handbook (7th Edition):

Zhao, Tianqi. “Catalytic formation of polycyclic aromatic hydrocarbons from acetylene over silicon carbide.” 2014. Web. 28 Mar 2020.

Vancouver:

Zhao T. Catalytic formation of polycyclic aromatic hydrocarbons from acetylene over silicon carbide. [Internet] [Masters thesis]. University of Hong Kong; 2014. [cited 2020 Mar 28]. Available from: Zhao, T. [趙天騏]. (2014). Catalytic formation of polycyclic aromatic hydrocarbons from acetylene over silicon carbide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5388030 ; http://dx.doi.org/10.5353/th_b5388030 ; http://hdl.handle.net/10722/208605.

Council of Science Editors:

Zhao T. Catalytic formation of polycyclic aromatic hydrocarbons from acetylene over silicon carbide. [Masters Thesis]. University of Hong Kong; 2014. Available from: Zhao, T. [趙天騏]. (2014). Catalytic formation of polycyclic aromatic hydrocarbons from acetylene over silicon carbide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5388030 ; http://dx.doi.org/10.5353/th_b5388030 ; http://hdl.handle.net/10722/208605


University of Hong Kong

19. Kuang, Liping. Asymmetric formal total synthesis of cortistatins A and J.

Degree: PhD, 2014, University of Hong Kong

published_or_final_version

Chemistry

Doctoral

Doctor of Philosophy

Subjects/Keywords: Alkaloids - Synthesis

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APA (6th Edition):

Kuang, L. (2014). Asymmetric formal total synthesis of cortistatins A and J. (Doctoral Dissertation). University of Hong Kong. Retrieved from Kuang, L. [况利平]. (2014). Asymmetric formal total synthesis of cortistatins A and J. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387972 ; http://dx.doi.org/10.5353/th_b5387972 ; http://hdl.handle.net/10722/208604

Chicago Manual of Style (16th Edition):

Kuang, Liping. “Asymmetric formal total synthesis of cortistatins A and J.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Kuang, L. [况利平]. (2014). Asymmetric formal total synthesis of cortistatins A and J. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387972 ; http://dx.doi.org/10.5353/th_b5387972 ; http://hdl.handle.net/10722/208604.

MLA Handbook (7th Edition):

Kuang, Liping. “Asymmetric formal total synthesis of cortistatins A and J.” 2014. Web. 28 Mar 2020.

Vancouver:

Kuang L. Asymmetric formal total synthesis of cortistatins A and J. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2020 Mar 28]. Available from: Kuang, L. [况利平]. (2014). Asymmetric formal total synthesis of cortistatins A and J. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387972 ; http://dx.doi.org/10.5353/th_b5387972 ; http://hdl.handle.net/10722/208604.

Council of Science Editors:

Kuang L. Asymmetric formal total synthesis of cortistatins A and J. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Kuang, L. [况利平]. (2014). Asymmetric formal total synthesis of cortistatins A and J. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387972 ; http://dx.doi.org/10.5353/th_b5387972 ; http://hdl.handle.net/10722/208604


University of Hong Kong

20. 徐明; Xu, Ming. Total synthesis of (+) and (-)- wilforonide, (+)-triptocallol, and analogs of triptolide.

Degree: PhD, 2000, University of Hong Kong

published_or_final_version

Chemistry

Doctoral

Doctor of Philosophy

Subjects/Keywords: Triptolide - Synthesis.

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APA (6th Edition):

徐明; Xu, M. (2000). Total synthesis of (+) and (-)- wilforonide, (+)-triptocallol, and analogs of triptolide. (Doctoral Dissertation). University of Hong Kong. Retrieved from Xu, M. [徐明]. (2000). Total synthesis of (+) and (-)- wilforonide, (+)-triptocallol, and analogs of triptolide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124255 ; http://dx.doi.org/10.5353/th_b3124255 ; http://hdl.handle.net/10722/35788

Chicago Manual of Style (16th Edition):

徐明; Xu, Ming. “Total synthesis of (+) and (-)- wilforonide, (+)-triptocallol, and analogs of triptolide.” 2000. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Xu, M. [徐明]. (2000). Total synthesis of (+) and (-)- wilforonide, (+)-triptocallol, and analogs of triptolide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124255 ; http://dx.doi.org/10.5353/th_b3124255 ; http://hdl.handle.net/10722/35788.

MLA Handbook (7th Edition):

徐明; Xu, Ming. “Total synthesis of (+) and (-)- wilforonide, (+)-triptocallol, and analogs of triptolide.” 2000. Web. 28 Mar 2020.

Vancouver:

徐明; Xu M. Total synthesis of (+) and (-)- wilforonide, (+)-triptocallol, and analogs of triptolide. [Internet] [Doctoral dissertation]. University of Hong Kong; 2000. [cited 2020 Mar 28]. Available from: Xu, M. [徐明]. (2000). Total synthesis of (+) and (-)- wilforonide, (+)-triptocallol, and analogs of triptolide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124255 ; http://dx.doi.org/10.5353/th_b3124255 ; http://hdl.handle.net/10722/35788.

Council of Science Editors:

徐明; Xu M. Total synthesis of (+) and (-)- wilforonide, (+)-triptocallol, and analogs of triptolide. [Doctoral Dissertation]. University of Hong Kong; 2000. Available from: Xu, M. [徐明]. (2000). Total synthesis of (+) and (-)- wilforonide, (+)-triptocallol, and analogs of triptolide. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124255 ; http://dx.doi.org/10.5353/th_b3124255 ; http://hdl.handle.net/10722/35788


University of Hong Kong

21. 侯斯健; Hou, Sijian. Syntheses and functionalization of block copolymers based on polystyrene-block-poly(4-vinylpyridine) and polystyrene-block-polyisoprene.

Degree: PhD, 1999, University of Hong Kong

published_or_final_version

Chemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Chan, WK.

Subjects/Keywords: Copolymers - Synthesis.

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APA (6th Edition):

侯斯健; Hou, S. (1999). Syntheses and functionalization of block copolymers based on polystyrene-block-poly(4-vinylpyridine) and polystyrene-block-polyisoprene. (Doctoral Dissertation). University of Hong Kong. Retrieved from Hou, S. [侯斯健]. (1999). Syntheses and functionalization of block copolymers based on polystyrene-block-poly(4-vinylpyridine) and polystyrene-block-polyisoprene. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124033 ; http://dx.doi.org/10.5353/th_b3124033 ; http://hdl.handle.net/10722/35950

Chicago Manual of Style (16th Edition):

侯斯健; Hou, Sijian. “Syntheses and functionalization of block copolymers based on polystyrene-block-poly(4-vinylpyridine) and polystyrene-block-polyisoprene.” 1999. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Hou, S. [侯斯健]. (1999). Syntheses and functionalization of block copolymers based on polystyrene-block-poly(4-vinylpyridine) and polystyrene-block-polyisoprene. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124033 ; http://dx.doi.org/10.5353/th_b3124033 ; http://hdl.handle.net/10722/35950.

MLA Handbook (7th Edition):

侯斯健; Hou, Sijian. “Syntheses and functionalization of block copolymers based on polystyrene-block-poly(4-vinylpyridine) and polystyrene-block-polyisoprene.” 1999. Web. 28 Mar 2020.

Vancouver:

侯斯健; Hou S. Syntheses and functionalization of block copolymers based on polystyrene-block-poly(4-vinylpyridine) and polystyrene-block-polyisoprene. [Internet] [Doctoral dissertation]. University of Hong Kong; 1999. [cited 2020 Mar 28]. Available from: Hou, S. [侯斯健]. (1999). Syntheses and functionalization of block copolymers based on polystyrene-block-poly(4-vinylpyridine) and polystyrene-block-polyisoprene. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124033 ; http://dx.doi.org/10.5353/th_b3124033 ; http://hdl.handle.net/10722/35950.

Council of Science Editors:

侯斯健; Hou S. Syntheses and functionalization of block copolymers based on polystyrene-block-poly(4-vinylpyridine) and polystyrene-block-polyisoprene. [Doctoral Dissertation]. University of Hong Kong; 1999. Available from: Hou, S. [侯斯健]. (1999). Syntheses and functionalization of block copolymers based on polystyrene-block-poly(4-vinylpyridine) and polystyrene-block-polyisoprene. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124033 ; http://dx.doi.org/10.5353/th_b3124033 ; http://hdl.handle.net/10722/35950


University of Hong Kong

22. 陳肇人; Chan, Diana. Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A.

Degree: PhD, 2016, University of Hong Kong

The first transannular (4+3) cycloadditions based on the activation of epoxy enolsilanes have been realized. Six macrocyclic epoxy ketones were converted to enolsilanes, then treated… (more)

Subjects/Keywords: Organic cyclic compounds - Synthesis

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APA (6th Edition):

陳肇人; Chan, D. (2016). Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/238343

Chicago Manual of Style (16th Edition):

陳肇人; Chan, Diana. “Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A.” 2016. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. http://hdl.handle.net/10722/238343.

MLA Handbook (7th Edition):

陳肇人; Chan, Diana. “Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A.” 2016. Web. 28 Mar 2020.

Vancouver:

陳肇人; Chan D. Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A. [Internet] [Doctoral dissertation]. University of Hong Kong; 2016. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10722/238343.

Council of Science Editors:

陳肇人; Chan D. Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A. [Doctoral Dissertation]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/238343


University of Hong Kong

23. Leakasindhu, Suleeporn. Synthesis of sanshools and related compounds.

Degree: M. Phil., 2016, University of Hong Kong

 Sanshools are naturally occurring aliphatic acid amide compounds found within plants from Zanthoxylum genus, the prickly ash genus of the rue family (Rutaceae). Sichuan pepper… (more)

Subjects/Keywords: Aliphatic compounds - Synthesis; Amides

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APA (6th Edition):

Leakasindhu, S. (2016). Synthesis of sanshools and related compounds. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/238357

Chicago Manual of Style (16th Edition):

Leakasindhu, Suleeporn. “Synthesis of sanshools and related compounds.” 2016. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. http://hdl.handle.net/10722/238357.

MLA Handbook (7th Edition):

Leakasindhu, Suleeporn. “Synthesis of sanshools and related compounds.” 2016. Web. 28 Mar 2020.

Vancouver:

Leakasindhu S. Synthesis of sanshools and related compounds. [Internet] [Masters thesis]. University of Hong Kong; 2016. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10722/238357.

Council of Science Editors:

Leakasindhu S. Synthesis of sanshools and related compounds. [Masters Thesis]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/238357


University of Hong Kong

24. 李智輝; Lee, Chi-fai. Synthesis of hibiscoquinone C and experiments in the synthesis of other naturally occurring quinones.

Degree: M. Phil., 1996, University of Hong Kong

published_or_final_version

Chemistry

Master

Master of Philosophy

Subjects/Keywords: Hibiscoquinone - Synthesis.

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APA (6th Edition):

李智輝; Lee, C. (1996). Synthesis of hibiscoquinone C and experiments in the synthesis of other naturally occurring quinones. (Masters Thesis). University of Hong Kong. Retrieved from Lee, C. [李智輝]. (1996). Synthesis of hibiscoquinone C and experiments in the synthesis of other naturally occurring quinones. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3121328 ; http://dx.doi.org/10.5353/th_b3121328 ; http://hdl.handle.net/10722/39343

Chicago Manual of Style (16th Edition):

李智輝; Lee, Chi-fai. “Synthesis of hibiscoquinone C and experiments in the synthesis of other naturally occurring quinones.” 1996. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Lee, C. [李智輝]. (1996). Synthesis of hibiscoquinone C and experiments in the synthesis of other naturally occurring quinones. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3121328 ; http://dx.doi.org/10.5353/th_b3121328 ; http://hdl.handle.net/10722/39343.

MLA Handbook (7th Edition):

李智輝; Lee, Chi-fai. “Synthesis of hibiscoquinone C and experiments in the synthesis of other naturally occurring quinones.” 1996. Web. 28 Mar 2020.

Vancouver:

李智輝; Lee C. Synthesis of hibiscoquinone C and experiments in the synthesis of other naturally occurring quinones. [Internet] [Masters thesis]. University of Hong Kong; 1996. [cited 2020 Mar 28]. Available from: Lee, C. [李智輝]. (1996). Synthesis of hibiscoquinone C and experiments in the synthesis of other naturally occurring quinones. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3121328 ; http://dx.doi.org/10.5353/th_b3121328 ; http://hdl.handle.net/10722/39343.

Council of Science Editors:

李智輝; Lee C. Synthesis of hibiscoquinone C and experiments in the synthesis of other naturally occurring quinones. [Masters Thesis]. University of Hong Kong; 1996. Available from: Lee, C. [李智輝]. (1996). Synthesis of hibiscoquinone C and experiments in the synthesis of other naturally occurring quinones. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3121328 ; http://dx.doi.org/10.5353/th_b3121328 ; http://hdl.handle.net/10722/39343


University of Hong Kong

25. 耿哲.; Geng, Zhe. Synthetic studies towards pseudolaric acids.

Degree: PhD, 2004, University of Hong Kong

published_or_final_version

Chemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Chiu, P.

Subjects/Keywords: Diterpenes - Synthesis.

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APA (6th Edition):

耿哲.; Geng, Z. (2004). Synthetic studies towards pseudolaric acids. (Doctoral Dissertation). University of Hong Kong. Retrieved from Geng, Z. [耿哲]. (2004). Synthetic studies towards pseudolaric acids. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124533 ; http://dx.doi.org/10.5353/th_b3124533 ; http://hdl.handle.net/10722/50423

Chicago Manual of Style (16th Edition):

耿哲.; Geng, Zhe. “Synthetic studies towards pseudolaric acids.” 2004. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Geng, Z. [耿哲]. (2004). Synthetic studies towards pseudolaric acids. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124533 ; http://dx.doi.org/10.5353/th_b3124533 ; http://hdl.handle.net/10722/50423.

MLA Handbook (7th Edition):

耿哲.; Geng, Zhe. “Synthetic studies towards pseudolaric acids.” 2004. Web. 28 Mar 2020.

Vancouver:

耿哲.; Geng Z. Synthetic studies towards pseudolaric acids. [Internet] [Doctoral dissertation]. University of Hong Kong; 2004. [cited 2020 Mar 28]. Available from: Geng, Z. [耿哲]. (2004). Synthetic studies towards pseudolaric acids. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124533 ; http://dx.doi.org/10.5353/th_b3124533 ; http://hdl.handle.net/10722/50423.

Council of Science Editors:

耿哲.; Geng Z. Synthetic studies towards pseudolaric acids. [Doctoral Dissertation]. University of Hong Kong; 2004. Available from: Geng, Z. [耿哲]. (2004). Synthetic studies towards pseudolaric acids. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124533 ; http://dx.doi.org/10.5353/th_b3124533 ; http://hdl.handle.net/10722/50423


University of Hong Kong

26. Li, Chi-ho. Synthesis of photosensitizing diblock copolymers for functionalizationof carbon nanotubes and their applications.

Degree: PhD, 2012, University of Hong Kong

Block copolymers containing pendant pyrene, terpyridine and poly(3- hexylthiophene) moieties with different block ratios and chain lengths were synthesized by reversible addition-fragmentation chain transfer (RAFT)… (more)

Subjects/Keywords: Copolymers - Synthesis.; Nanotubes - Carbon content.

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APA (6th Edition):

Li, C. (2012). Synthesis of photosensitizing diblock copolymers for functionalizationof carbon nanotubes and their applications. (Doctoral Dissertation). University of Hong Kong. Retrieved from Li, C. [李志豪]. (2012). Synthesis of photosensitizing diblock copolymers for functionalization of carbon nanotubes and their applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4786937 ; http://dx.doi.org/10.5353/th_b4786937 ; http://hdl.handle.net/10722/183040

Chicago Manual of Style (16th Edition):

Li, Chi-ho. “Synthesis of photosensitizing diblock copolymers for functionalizationof carbon nanotubes and their applications.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Li, C. [李志豪]. (2012). Synthesis of photosensitizing diblock copolymers for functionalization of carbon nanotubes and their applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4786937 ; http://dx.doi.org/10.5353/th_b4786937 ; http://hdl.handle.net/10722/183040.

MLA Handbook (7th Edition):

Li, Chi-ho. “Synthesis of photosensitizing diblock copolymers for functionalizationof carbon nanotubes and their applications.” 2012. Web. 28 Mar 2020.

Vancouver:

Li C. Synthesis of photosensitizing diblock copolymers for functionalizationof carbon nanotubes and their applications. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Li, C. [李志豪]. (2012). Synthesis of photosensitizing diblock copolymers for functionalization of carbon nanotubes and their applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4786937 ; http://dx.doi.org/10.5353/th_b4786937 ; http://hdl.handle.net/10722/183040.

Council of Science Editors:

Li C. Synthesis of photosensitizing diblock copolymers for functionalizationof carbon nanotubes and their applications. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Li, C. [李志豪]. (2012). Synthesis of photosensitizing diblock copolymers for functionalization of carbon nanotubes and their applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4786937 ; http://dx.doi.org/10.5353/th_b4786937 ; http://hdl.handle.net/10722/183040


University of Hong Kong

27. Guo, Jiawen. Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction.

Degree: M. Phil., 2013, University of Hong Kong

Recently, during the past10 years, with the intensified attention paid to the environment and industrial development, there has been growing interest in organocatalysis. One important… (more)

Subjects/Keywords: Chemistry, Organic; Catalysts - Synthesis; Catalysis

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APA (6th Edition):

Guo, J. (2013). Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. (Masters Thesis). University of Hong Kong. Retrieved from Guo, J. [郭嘉雯]. (2013). Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153730 ; http://dx.doi.org/10.5353/th_b5153730 ; http://hdl.handle.net/10722/196023

Chicago Manual of Style (16th Edition):

Guo, Jiawen. “Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction.” 2013. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Guo, J. [郭嘉雯]. (2013). Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153730 ; http://dx.doi.org/10.5353/th_b5153730 ; http://hdl.handle.net/10722/196023.

MLA Handbook (7th Edition):

Guo, Jiawen. “Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction.” 2013. Web. 28 Mar 2020.

Vancouver:

Guo J. Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. [Internet] [Masters thesis]. University of Hong Kong; 2013. [cited 2020 Mar 28]. Available from: Guo, J. [郭嘉雯]. (2013). Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153730 ; http://dx.doi.org/10.5353/th_b5153730 ; http://hdl.handle.net/10722/196023.

Council of Science Editors:

Guo J. Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. [Masters Thesis]. University of Hong Kong; 2013. Available from: Guo, J. [郭嘉雯]. (2013). Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153730 ; http://dx.doi.org/10.5353/th_b5153730 ; http://hdl.handle.net/10722/196023


University of Hong Kong

28. 鍾亦琛; Chung, Yik-sham, Clive. Design, synthesis, photophysics and self-assembly study of platinum (II) terpyridine complexes and their utilization as stimuli-responsive smart materials and probes for molecules and macromolecules of biological interest.

Degree: PhD, 2013, University of Hong Kong

 A series of water-soluble platinum(II) terpyridine complexes with functionalized alkynyl ligands and a boronic acid-containing polymer, PAAPBA, have been synthesized and characterized. The photophysical and… (more)

Subjects/Keywords: Platinum compounds - Synthesis; Photochemistry; Pyridine; Complex compounds - Synthesis

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APA (6th Edition):

鍾亦琛; Chung, Yik-sham, C. (2013). Design, synthesis, photophysics and self-assembly study of platinum (II) terpyridine complexes and their utilization as stimuli-responsive smart materials and probes for molecules and macromolecules of biological interest. (Doctoral Dissertation). University of Hong Kong. Retrieved from Chung, Y. C. [鍾亦琛]. (2013). Design, synthesis, photophysics and self-assembly study of platinum (II) terpyridine complexes and their utilization as stimuli-responsive smart materials and probes for molecules and macromolecules of biological interest. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5016243 ; http://dx.doi.org/10.5353/th_b5016243 ; http://hdl.handle.net/10722/208570

Chicago Manual of Style (16th Edition):

鍾亦琛; Chung, Yik-sham, Clive. “Design, synthesis, photophysics and self-assembly study of platinum (II) terpyridine complexes and their utilization as stimuli-responsive smart materials and probes for molecules and macromolecules of biological interest.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Chung, Y. C. [鍾亦琛]. (2013). Design, synthesis, photophysics and self-assembly study of platinum (II) terpyridine complexes and their utilization as stimuli-responsive smart materials and probes for molecules and macromolecules of biological interest. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5016243 ; http://dx.doi.org/10.5353/th_b5016243 ; http://hdl.handle.net/10722/208570.

MLA Handbook (7th Edition):

鍾亦琛; Chung, Yik-sham, Clive. “Design, synthesis, photophysics and self-assembly study of platinum (II) terpyridine complexes and their utilization as stimuli-responsive smart materials and probes for molecules and macromolecules of biological interest.” 2013. Web. 28 Mar 2020.

Vancouver:

鍾亦琛; Chung, Yik-sham C. Design, synthesis, photophysics and self-assembly study of platinum (II) terpyridine complexes and their utilization as stimuli-responsive smart materials and probes for molecules and macromolecules of biological interest. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2020 Mar 28]. Available from: Chung, Y. C. [鍾亦琛]. (2013). Design, synthesis, photophysics and self-assembly study of platinum (II) terpyridine complexes and their utilization as stimuli-responsive smart materials and probes for molecules and macromolecules of biological interest. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5016243 ; http://dx.doi.org/10.5353/th_b5016243 ; http://hdl.handle.net/10722/208570.

Council of Science Editors:

鍾亦琛; Chung, Yik-sham C. Design, synthesis, photophysics and self-assembly study of platinum (II) terpyridine complexes and their utilization as stimuli-responsive smart materials and probes for molecules and macromolecules of biological interest. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Chung, Y. C. [鍾亦琛]. (2013). Design, synthesis, photophysics and self-assembly study of platinum (II) terpyridine complexes and their utilization as stimuli-responsive smart materials and probes for molecules and macromolecules of biological interest. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5016243 ; http://dx.doi.org/10.5353/th_b5016243 ; http://hdl.handle.net/10722/208570


University of Hong Kong

29. 張偉基.; Cheung, Wai-kei. Low band-gap donor-acceptor polymers and heterolyptic ruthenium complex containing polymers for photovoltaic applications.

Degree: M. Phil., 2012, University of Hong Kong

A series of low band-gap conjugated polymers with intramolecular charge transfer properties were synthesized and bulk heterojunction devices based on these polymers were fabricated. The… (more)

Subjects/Keywords: Organic compounds - Synthesis.; Conjugated polymers.; Ruthenium compounds - Synthesis.

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APA (6th Edition):

張偉基.; Cheung, W. (2012). Low band-gap donor-acceptor polymers and heterolyptic ruthenium complex containing polymers for photovoltaic applications. (Masters Thesis). University of Hong Kong. Retrieved from Cheung, W. [張偉基]. (2012). Low band-gap donor-acceptor polymers and heterolyptic ruthenium complex containing polymers for photovoltaic applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4775300 ; http://dx.doi.org/10.5353/th_b4775300 ; http://hdl.handle.net/10722/174480

Chicago Manual of Style (16th Edition):

張偉基.; Cheung, Wai-kei. “Low band-gap donor-acceptor polymers and heterolyptic ruthenium complex containing polymers for photovoltaic applications.” 2012. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Cheung, W. [張偉基]. (2012). Low band-gap donor-acceptor polymers and heterolyptic ruthenium complex containing polymers for photovoltaic applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4775300 ; http://dx.doi.org/10.5353/th_b4775300 ; http://hdl.handle.net/10722/174480.

MLA Handbook (7th Edition):

張偉基.; Cheung, Wai-kei. “Low band-gap donor-acceptor polymers and heterolyptic ruthenium complex containing polymers for photovoltaic applications.” 2012. Web. 28 Mar 2020.

Vancouver:

張偉基.; Cheung W. Low band-gap donor-acceptor polymers and heterolyptic ruthenium complex containing polymers for photovoltaic applications. [Internet] [Masters thesis]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Cheung, W. [張偉基]. (2012). Low band-gap donor-acceptor polymers and heterolyptic ruthenium complex containing polymers for photovoltaic applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4775300 ; http://dx.doi.org/10.5353/th_b4775300 ; http://hdl.handle.net/10722/174480.

Council of Science Editors:

張偉基.; Cheung W. Low band-gap donor-acceptor polymers and heterolyptic ruthenium complex containing polymers for photovoltaic applications. [Masters Thesis]. University of Hong Kong; 2012. Available from: Cheung, W. [張偉基]. (2012). Low band-gap donor-acceptor polymers and heterolyptic ruthenium complex containing polymers for photovoltaic applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4775300 ; http://dx.doi.org/10.5353/th_b4775300 ; http://hdl.handle.net/10722/174480


University of Hong Kong

30. 陳凱耀.; Chan, Hoi-yiu. Design and synthesis of luminescent mono- and dinuclear platinum(II) alkynyl terpyridine complexes: fromphotophysics to aggregation and self-assembly.

Degree: PhD, 2006, University of Hong Kong

abstract

published_or_final_version

Chemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Yam, VWW.

Subjects/Keywords: Pyridine - Synthesis.; Platinum compounds - Synthesis.

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

陳凱耀.; Chan, H. (2006). Design and synthesis of luminescent mono- and dinuclear platinum(II) alkynyl terpyridine complexes: fromphotophysics to aggregation and self-assembly. (Doctoral Dissertation). University of Hong Kong. Retrieved from Chan, H. [陳凱耀]. (2006). Design and synthesis of luminescent mono- and dinuclear platinum(II) alkynyl terpyridine complexes : from photophysics to aggregation and self-assembly. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3692923 ; http://dx.doi.org/10.5353/th_b3692923 ; http://hdl.handle.net/10722/50336

Chicago Manual of Style (16th Edition):

陳凱耀.; Chan, Hoi-yiu. “Design and synthesis of luminescent mono- and dinuclear platinum(II) alkynyl terpyridine complexes: fromphotophysics to aggregation and self-assembly.” 2006. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Chan, H. [陳凱耀]. (2006). Design and synthesis of luminescent mono- and dinuclear platinum(II) alkynyl terpyridine complexes : from photophysics to aggregation and self-assembly. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3692923 ; http://dx.doi.org/10.5353/th_b3692923 ; http://hdl.handle.net/10722/50336.

MLA Handbook (7th Edition):

陳凱耀.; Chan, Hoi-yiu. “Design and synthesis of luminescent mono- and dinuclear platinum(II) alkynyl terpyridine complexes: fromphotophysics to aggregation and self-assembly.” 2006. Web. 28 Mar 2020.

Vancouver:

陳凱耀.; Chan H. Design and synthesis of luminescent mono- and dinuclear platinum(II) alkynyl terpyridine complexes: fromphotophysics to aggregation and self-assembly. [Internet] [Doctoral dissertation]. University of Hong Kong; 2006. [cited 2020 Mar 28]. Available from: Chan, H. [陳凱耀]. (2006). Design and synthesis of luminescent mono- and dinuclear platinum(II) alkynyl terpyridine complexes : from photophysics to aggregation and self-assembly. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3692923 ; http://dx.doi.org/10.5353/th_b3692923 ; http://hdl.handle.net/10722/50336.

Council of Science Editors:

陳凱耀.; Chan H. Design and synthesis of luminescent mono- and dinuclear platinum(II) alkynyl terpyridine complexes: fromphotophysics to aggregation and self-assembly. [Doctoral Dissertation]. University of Hong Kong; 2006. Available from: Chan, H. [陳凱耀]. (2006). Design and synthesis of luminescent mono- and dinuclear platinum(II) alkynyl terpyridine complexes : from photophysics to aggregation and self-assembly. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3692923 ; http://dx.doi.org/10.5353/th_b3692923 ; http://hdl.handle.net/10722/50336

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