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You searched for subject:(Hydrosilylation). Showing records 1 – 30 of 93 total matches.

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University of Edinburgh

1. Challinor, Amy Jane. Beyond organometallic in situ activation : the influence of the counter ion in base metal catalysis.

Degree: PhD, 2017, University of Edinburgh

 The amine-activated iron-catalysed hydrosilylation of alkenes and alkynes has been developed, and has been found to selectively provide the anti-Markovnikov product. It was established that… (more)

Subjects/Keywords: iron cataylsis; hydrosilylation

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APA (6th Edition):

Challinor, A. J. (2017). Beyond organometallic in situ activation : the influence of the counter ion in base metal catalysis. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28810

Chicago Manual of Style (16th Edition):

Challinor, Amy Jane. “Beyond organometallic in situ activation : the influence of the counter ion in base metal catalysis.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed March 28, 2020. http://hdl.handle.net/1842/28810.

MLA Handbook (7th Edition):

Challinor, Amy Jane. “Beyond organometallic in situ activation : the influence of the counter ion in base metal catalysis.” 2017. Web. 28 Mar 2020.

Vancouver:

Challinor AJ. Beyond organometallic in situ activation : the influence of the counter ion in base metal catalysis. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/1842/28810.

Council of Science Editors:

Challinor AJ. Beyond organometallic in situ activation : the influence of the counter ion in base metal catalysis. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28810


University of Victoria

2. Hooper, Richard. Synthesis, characterization and group modification of carbosilane based dendrimers.

Degree: Department of Chemistry, 2017, University of Victoria

 Carbosilane dendrimers have been prepared via iterative hydrosilylation/alkenylation reactions using a variety of chlorosilanes (HSiMe₃₋nC1n)and alkenyl nucleophiles (CH₂=CHCH₂MgBr and CH₂=CHMgBr). Characterization by multinuclear NMR spectroscopy… (more)

Subjects/Keywords: Hydrosilylation; Dendrimers; Chemistry, Organic

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APA (6th Edition):

Hooper, R. (2017). Synthesis, characterization and group modification of carbosilane based dendrimers. (Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/8290

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hooper, Richard. “Synthesis, characterization and group modification of carbosilane based dendrimers.” 2017. Thesis, University of Victoria. Accessed March 28, 2020. http://hdl.handle.net/1828/8290.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hooper, Richard. “Synthesis, characterization and group modification of carbosilane based dendrimers.” 2017. Web. 28 Mar 2020.

Vancouver:

Hooper R. Synthesis, characterization and group modification of carbosilane based dendrimers. [Internet] [Thesis]. University of Victoria; 2017. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/1828/8290.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hooper R. Synthesis, characterization and group modification of carbosilane based dendrimers. [Thesis]. University of Victoria; 2017. Available from: http://hdl.handle.net/1828/8290

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Edinburgh

3. Carney, Jonathan Robert. Manganese-catalysed hydrofunctionalisation of alkenes.

Degree: PhD, 2019, University of Edinburgh

 The development of new first-row transition metal catalysts as both replacements for precious metals catalysts and in the search for novel reactivity is a crucial… (more)

Subjects/Keywords: manganese; catalysis; hydrosilylation; hydroboration

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APA (6th Edition):

Carney, J. R. (2019). Manganese-catalysed hydrofunctionalisation of alkenes. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/35699

Chicago Manual of Style (16th Edition):

Carney, Jonathan Robert. “Manganese-catalysed hydrofunctionalisation of alkenes.” 2019. Doctoral Dissertation, University of Edinburgh. Accessed March 28, 2020. http://hdl.handle.net/1842/35699.

MLA Handbook (7th Edition):

Carney, Jonathan Robert. “Manganese-catalysed hydrofunctionalisation of alkenes.” 2019. Web. 28 Mar 2020.

Vancouver:

Carney JR. Manganese-catalysed hydrofunctionalisation of alkenes. [Internet] [Doctoral dissertation]. University of Edinburgh; 2019. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/1842/35699.

Council of Science Editors:

Carney JR. Manganese-catalysed hydrofunctionalisation of alkenes. [Doctoral Dissertation]. University of Edinburgh; 2019. Available from: http://hdl.handle.net/1842/35699

4. Galeandro-Diamant, Thomas. Metal nanoparticles as catalysts for alkene hydrosilylation : Nanoparticules de métaux comme catalyseurs pour l'hydrosilylation des alcènes.

Degree: Docteur es, Chimie, 2016, Lyon

L'hydrosilylation des alcènes est une méthode cruciale de formation de liaisons carbone-silicium. Elle est utilisée industriellement pour la production de fluides silicones fonctionnels et d'élastomères… (more)

Subjects/Keywords: Nanoparticules; Métaux; Hydrosilylation; Alcènes; Silicones; Nanoparticles; Metals; Hydrosilylation; Alkenes; Silicones; 660

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APA (6th Edition):

Galeandro-Diamant, T. (2016). Metal nanoparticles as catalysts for alkene hydrosilylation : Nanoparticules de métaux comme catalyseurs pour l'hydrosilylation des alcènes. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2016LYSE1285

Chicago Manual of Style (16th Edition):

Galeandro-Diamant, Thomas. “Metal nanoparticles as catalysts for alkene hydrosilylation : Nanoparticules de métaux comme catalyseurs pour l'hydrosilylation des alcènes.” 2016. Doctoral Dissertation, Lyon. Accessed March 28, 2020. http://www.theses.fr/2016LYSE1285.

MLA Handbook (7th Edition):

Galeandro-Diamant, Thomas. “Metal nanoparticles as catalysts for alkene hydrosilylation : Nanoparticules de métaux comme catalyseurs pour l'hydrosilylation des alcènes.” 2016. Web. 28 Mar 2020.

Vancouver:

Galeandro-Diamant T. Metal nanoparticles as catalysts for alkene hydrosilylation : Nanoparticules de métaux comme catalyseurs pour l'hydrosilylation des alcènes. [Internet] [Doctoral dissertation]. Lyon; 2016. [cited 2020 Mar 28]. Available from: http://www.theses.fr/2016LYSE1285.

Council of Science Editors:

Galeandro-Diamant T. Metal nanoparticles as catalysts for alkene hydrosilylation : Nanoparticules de métaux comme catalyseurs pour l'hydrosilylation des alcènes. [Doctoral Dissertation]. Lyon; 2016. Available from: http://www.theses.fr/2016LYSE1285

5. Monsigny, Louis. Catalyseurs d’hydrosilylation pour la réduction de liaisons C-O dans les polymères oxygénés : Hydrosilylation Catalysts for the Reduction of C-O bonds in Oxygenated Polymers.

Degree: Docteur es, Chimie, 2019, Université Paris-Saclay (ComUE)

L’objectif principal de cette thèse a été de développer de nouveaux systèmes catalytiques efficaces pour la dépolymérisation de la biomasse et des plastiques. La stratégie… (more)

Subjects/Keywords: Catalyse; Biomasse; Lignine; Plastique; Hydrosilylation; Catalysis; Biomass; Lignin; Plastic; Hydrosilylation

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APA (6th Edition):

Monsigny, L. (2019). Catalyseurs d’hydrosilylation pour la réduction de liaisons C-O dans les polymères oxygénés : Hydrosilylation Catalysts for the Reduction of C-O bonds in Oxygenated Polymers. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS026

Chicago Manual of Style (16th Edition):

Monsigny, Louis. “Catalyseurs d’hydrosilylation pour la réduction de liaisons C-O dans les polymères oxygénés : Hydrosilylation Catalysts for the Reduction of C-O bonds in Oxygenated Polymers.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed March 28, 2020. http://www.theses.fr/2019SACLS026.

MLA Handbook (7th Edition):

Monsigny, Louis. “Catalyseurs d’hydrosilylation pour la réduction de liaisons C-O dans les polymères oxygénés : Hydrosilylation Catalysts for the Reduction of C-O bonds in Oxygenated Polymers.” 2019. Web. 28 Mar 2020.

Vancouver:

Monsigny L. Catalyseurs d’hydrosilylation pour la réduction de liaisons C-O dans les polymères oxygénés : Hydrosilylation Catalysts for the Reduction of C-O bonds in Oxygenated Polymers. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Mar 28]. Available from: http://www.theses.fr/2019SACLS026.

Council of Science Editors:

Monsigny L. Catalyseurs d’hydrosilylation pour la réduction de liaisons C-O dans les polymères oxygénés : Hydrosilylation Catalysts for the Reduction of C-O bonds in Oxygenated Polymers. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS026


University of California – San Diego

6. Spence, Daniel Patrick. Hydrosilylation of Imines Using a Ni(0) Catalyst.

Degree: Chemistry, 2016, University of California – San Diego

 The following herein introduces a Ni(0) catalyst that effectively does hydrosilylation of imines to form the corresponding aminosilanes which are of interest in the electronics… (more)

Subjects/Keywords: Chemistry; hydrosilylation; imines; Ni(0); nickel

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APA (6th Edition):

Spence, D. P. (2016). Hydrosilylation of Imines Using a Ni(0) Catalyst. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/3rk405ww

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Spence, Daniel Patrick. “Hydrosilylation of Imines Using a Ni(0) Catalyst.” 2016. Thesis, University of California – San Diego. Accessed March 28, 2020. http://www.escholarship.org/uc/item/3rk405ww.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Spence, Daniel Patrick. “Hydrosilylation of Imines Using a Ni(0) Catalyst.” 2016. Web. 28 Mar 2020.

Vancouver:

Spence DP. Hydrosilylation of Imines Using a Ni(0) Catalyst. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2020 Mar 28]. Available from: http://www.escholarship.org/uc/item/3rk405ww.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Spence DP. Hydrosilylation of Imines Using a Ni(0) Catalyst. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/3rk405ww

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


The Ohio State University

7. Raya, Balaram. Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene.

Degree: PhD, Chemistry, 2016, The Ohio State University

 Organic reactions catalyzed by metal complexes are an effective way to improve atom economy and environmental friendliness for many synthetic transformations. Among the various synthetic… (more)

Subjects/Keywords: Organic Chemistry; Cyclization, Hydrosilylation, Hydrogenation and Hydrovinylation

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APA (6th Edition):

Raya, B. (2016). Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1480602126518218

Chicago Manual of Style (16th Edition):

Raya, Balaram. “Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene.” 2016. Doctoral Dissertation, The Ohio State University. Accessed March 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1480602126518218.

MLA Handbook (7th Edition):

Raya, Balaram. “Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene.” 2016. Web. 28 Mar 2020.

Vancouver:

Raya B. Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2020 Mar 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1480602126518218.

Council of Science Editors:

Raya B. Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1480602126518218


University of Edinburgh

8. Zhu, Kailong. Iron-catalysed hydride and radical transfer reactions.

Degree: PhD, 2017, University of Edinburgh

 Iron-catalysed carbonyl reduction, nitro reduction, formal hydroamination, and the radical alkenylation of alkyl halides have been developed. A Simple, easy-to-make, air- and moisture-stable iron(III) amine-bis(phenolate)… (more)

Subjects/Keywords: iron catalysis; carbonyl; nitro compounds; hydrosilylation; radical

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APA (6th Edition):

Zhu, K. (2017). Iron-catalysed hydride and radical transfer reactions. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28732

Chicago Manual of Style (16th Edition):

Zhu, Kailong. “Iron-catalysed hydride and radical transfer reactions.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed March 28, 2020. http://hdl.handle.net/1842/28732.

MLA Handbook (7th Edition):

Zhu, Kailong. “Iron-catalysed hydride and radical transfer reactions.” 2017. Web. 28 Mar 2020.

Vancouver:

Zhu K. Iron-catalysed hydride and radical transfer reactions. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/1842/28732.

Council of Science Editors:

Zhu K. Iron-catalysed hydride and radical transfer reactions. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28732


Princeton University

9. Hoyt, Jordan. Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions .

Degree: PhD, 2015, Princeton University

 The synthesis of a new bis(imino)pyridine iron dinitogen compound, (iPr(tb)PDI)Fe(N2)2, was undertaken in order to explore the effect of restricting imine dissociation on catalysis. While… (more)

Subjects/Keywords: Catalysis; Cycloaddition; Cycloisomerization; Hydrogenation; Hydrosilylation; Iron

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APA (6th Edition):

Hoyt, J. (2015). Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp0112579v570

Chicago Manual of Style (16th Edition):

Hoyt, Jordan. “Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions .” 2015. Doctoral Dissertation, Princeton University. Accessed March 28, 2020. http://arks.princeton.edu/ark:/88435/dsp0112579v570.

MLA Handbook (7th Edition):

Hoyt, Jordan. “Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions .” 2015. Web. 28 Mar 2020.

Vancouver:

Hoyt J. Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions . [Internet] [Doctoral dissertation]. Princeton University; 2015. [cited 2020 Mar 28]. Available from: http://arks.princeton.edu/ark:/88435/dsp0112579v570.

Council of Science Editors:

Hoyt J. Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions . [Doctoral Dissertation]. Princeton University; 2015. Available from: http://arks.princeton.edu/ark:/88435/dsp0112579v570


Rutgers University

10. Terrado, Rhyan Joseph, 1978. Troticene lithiation and platinum-catalyzed hydrosilylation using dimethylsilyl- troticene and ferrocene derivatives:.

Degree: PhD, Chemistry, 2009, Rutgers University

The lithiation of troticene was studied. Monolithiation of troticene at 0 °C preferentially occurred at the cycloheptatrienyl (Cht) ligand,1,2 while monolithiation at room temperature preferentially… (more)

Subjects/Keywords: Organolithium compounds; Hydrosilylation

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APA (6th Edition):

Terrado, Rhyan Joseph, 1. (2009). Troticene lithiation and platinum-catalyzed hydrosilylation using dimethylsilyl- troticene and ferrocene derivatives:. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10002600001.ETD.000051319

Chicago Manual of Style (16th Edition):

Terrado, Rhyan Joseph, 1978. “Troticene lithiation and platinum-catalyzed hydrosilylation using dimethylsilyl- troticene and ferrocene derivatives:.” 2009. Doctoral Dissertation, Rutgers University. Accessed March 28, 2020. http://hdl.rutgers.edu/1782.2/rucore10002600001.ETD.000051319.

MLA Handbook (7th Edition):

Terrado, Rhyan Joseph, 1978. “Troticene lithiation and platinum-catalyzed hydrosilylation using dimethylsilyl- troticene and ferrocene derivatives:.” 2009. Web. 28 Mar 2020.

Vancouver:

Terrado, Rhyan Joseph 1. Troticene lithiation and platinum-catalyzed hydrosilylation using dimethylsilyl- troticene and ferrocene derivatives:. [Internet] [Doctoral dissertation]. Rutgers University; 2009. [cited 2020 Mar 28]. Available from: http://hdl.rutgers.edu/1782.2/rucore10002600001.ETD.000051319.

Council of Science Editors:

Terrado, Rhyan Joseph 1. Troticene lithiation and platinum-catalyzed hydrosilylation using dimethylsilyl- troticene and ferrocene derivatives:. [Doctoral Dissertation]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10002600001.ETD.000051319


University of Illinois – Urbana-Champaign

11. Chu, Wan-Yi. Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights.

Degree: PhD, Chemistry, 2016, University of Illinois – Urbana-Champaign

 The utility of transition metal catalysts has greatly expanded the scope of organic reactions. Historically, homogenous catalysis is dominated by platinum group metals (PGMs) due… (more)

Subjects/Keywords: organometallic compounds; hydrosilylation; catalysis; non-innocent ligands

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APA (6th Edition):

Chu, W. (2016). Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90874

Chicago Manual of Style (16th Edition):

Chu, Wan-Yi. “Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed March 28, 2020. http://hdl.handle.net/2142/90874.

MLA Handbook (7th Edition):

Chu, Wan-Yi. “Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights.” 2016. Web. 28 Mar 2020.

Vancouver:

Chu W. Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/2142/90874.

Council of Science Editors:

Chu W. Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90874


Université Paris-Sud – Paris XI

12. Blondiaux, Enguerrand. Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules.

Degree: Docteur es, Chimie, 2015, Université Paris-Sud – Paris XI

Les ressources carbonées fossiles (pétrole, charbon, gaz) couvrent 85 % des besoins énergétiques mondiaux et servent de matières premières pour 95 % des consommables chimiques… (more)

Subjects/Keywords: CO2; Amines; Organocatalyse; Réduction; Hydrosilylation; Hydroboration; CO2; Amines; Organocatalysis; Reduction; Hydrosilylation; Hydroboration

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APA (6th Edition):

Blondiaux, E. (2015). Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2015PA112151

Chicago Manual of Style (16th Edition):

Blondiaux, Enguerrand. “Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules.” 2015. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed March 28, 2020. http://www.theses.fr/2015PA112151.

MLA Handbook (7th Edition):

Blondiaux, Enguerrand. “Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules.” 2015. Web. 28 Mar 2020.

Vancouver:

Blondiaux E. Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2015. [cited 2020 Mar 28]. Available from: http://www.theses.fr/2015PA112151.

Council of Science Editors:

Blondiaux E. Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2015. Available from: http://www.theses.fr/2015PA112151

13. Larribe, Gabriel. Synthèse de mousses silicone par la voie émulsion : Silicone foams foram emulsions.

Degree: Docteur es, Chimie des matériaux, 2018, Lyon

La première partie de ce travail recense les différentes technologies permettant de générer des mousses silicone. Des généralités sur les émulsions, sur la génération de… (more)

Subjects/Keywords: Matériaux; Mousse; Silicones; Emulsion; Réticulation; Hydrosilylation; Materials; Foam; Silicon; Emulsion; Crosslinking; Hydrosilylation; 620.192 072

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APA (6th Edition):

Larribe, G. (2018). Synthèse de mousses silicone par la voie émulsion : Silicone foams foram emulsions. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2018LYSEI032

Chicago Manual of Style (16th Edition):

Larribe, Gabriel. “Synthèse de mousses silicone par la voie émulsion : Silicone foams foram emulsions.” 2018. Doctoral Dissertation, Lyon. Accessed March 28, 2020. http://www.theses.fr/2018LYSEI032.

MLA Handbook (7th Edition):

Larribe, Gabriel. “Synthèse de mousses silicone par la voie émulsion : Silicone foams foram emulsions.” 2018. Web. 28 Mar 2020.

Vancouver:

Larribe G. Synthèse de mousses silicone par la voie émulsion : Silicone foams foram emulsions. [Internet] [Doctoral dissertation]. Lyon; 2018. [cited 2020 Mar 28]. Available from: http://www.theses.fr/2018LYSEI032.

Council of Science Editors:

Larribe G. Synthèse de mousses silicone par la voie émulsion : Silicone foams foram emulsions. [Doctoral Dissertation]. Lyon; 2018. Available from: http://www.theses.fr/2018LYSEI032

14. Aschl, Timothy. Biochips based on silicon for detecting the interaction between aptamers and pathogens : Biocapteurs sur silicium pour la détection des interactions aptamères / agents pathogènes.

Degree: Docteur es, Chimie, 2016, Université Paris-Saclay (ComUE)

La détection rapide et sensible des agents pathogènes est d’une très grande importance pour la biosécurité. Les biopuces sont bien adaptées à cet effet, car… (more)

Subjects/Keywords: Biopuce; Aptamère; Pathogène; Ochratoxine A; Hydrosilylation; Biochip; Aptamer; Pathogen; Ochratoxin A; Hydrosilylation

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APA (6th Edition):

Aschl, T. (2016). Biochips based on silicon for detecting the interaction between aptamers and pathogens : Biocapteurs sur silicium pour la détection des interactions aptamères / agents pathogènes. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2016SACLX103

Chicago Manual of Style (16th Edition):

Aschl, Timothy. “Biochips based on silicon for detecting the interaction between aptamers and pathogens : Biocapteurs sur silicium pour la détection des interactions aptamères / agents pathogènes.” 2016. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed March 28, 2020. http://www.theses.fr/2016SACLX103.

MLA Handbook (7th Edition):

Aschl, Timothy. “Biochips based on silicon for detecting the interaction between aptamers and pathogens : Biocapteurs sur silicium pour la détection des interactions aptamères / agents pathogènes.” 2016. Web. 28 Mar 2020.

Vancouver:

Aschl T. Biochips based on silicon for detecting the interaction between aptamers and pathogens : Biocapteurs sur silicium pour la détection des interactions aptamères / agents pathogènes. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2016. [cited 2020 Mar 28]. Available from: http://www.theses.fr/2016SACLX103.

Council of Science Editors:

Aschl T. Biochips based on silicon for detecting the interaction between aptamers and pathogens : Biocapteurs sur silicium pour la détection des interactions aptamères / agents pathogènes. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2016. Available from: http://www.theses.fr/2016SACLX103

15. Li, Bin. Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II).

Degree: Docteur es, Chimie, 2013, Rennes 1

Dans ce travail de recherche, la synthèse de complexes de ruthénium cyclometallés a été effectuée à partir d'imines, 2-phénylpyridine, 2-phényloxazoline, phénylpyrazole, et benzo[h]quinoline par réaction… (more)

Subjects/Keywords: Ruthénium; Catalyse; Activation C-H; Couplages mixtes; Hydrosilylation; Ruthenium; Catalysis; C-H bond activation; Cross-couplings; Hydrosilylation

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APA (6th Edition):

Li, B. (2013). Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II). (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2013REN1S114

Chicago Manual of Style (16th Edition):

Li, Bin. “Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II).” 2013. Doctoral Dissertation, Rennes 1. Accessed March 28, 2020. http://www.theses.fr/2013REN1S114.

MLA Handbook (7th Edition):

Li, Bin. “Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II).” 2013. Web. 28 Mar 2020.

Vancouver:

Li B. Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II). [Internet] [Doctoral dissertation]. Rennes 1; 2013. [cited 2020 Mar 28]. Available from: http://www.theses.fr/2013REN1S114.

Council of Science Editors:

Li B. Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II). [Doctoral Dissertation]. Rennes 1; 2013. Available from: http://www.theses.fr/2013REN1S114


INP Toulouse

16. Fustier, Céline. Développement d'un réacteur intensifié en Carbure de Silicium pour la transposition en continu de réactions d'hydrosilylation : Development of Silicon Carbide equipments for the transposition of hydrosilylation reactions from batch to continuous.

Degree: Docteur es, Génie des procédés et de l'environnement, 2012, INP Toulouse

De nos jours, les limites du réacteur batch, outil conventionnel de l'industrie de la chimie fine, en termes de transfert thermique et de transfert de… (more)

Subjects/Keywords: Intensification des procédés; Réacteurs-échangeurs; Carbure de silicium; Hydrosilylation; Process Intensification; Heat exchanger reactor; Silicon carbide; Hydrosilylation

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APA (6th Edition):

Fustier, C. (2012). Développement d'un réacteur intensifié en Carbure de Silicium pour la transposition en continu de réactions d'hydrosilylation : Development of Silicon Carbide equipments for the transposition of hydrosilylation reactions from batch to continuous. (Doctoral Dissertation). INP Toulouse. Retrieved from http://www.theses.fr/2012INPT0142

Chicago Manual of Style (16th Edition):

Fustier, Céline. “Développement d'un réacteur intensifié en Carbure de Silicium pour la transposition en continu de réactions d'hydrosilylation : Development of Silicon Carbide equipments for the transposition of hydrosilylation reactions from batch to continuous.” 2012. Doctoral Dissertation, INP Toulouse. Accessed March 28, 2020. http://www.theses.fr/2012INPT0142.

MLA Handbook (7th Edition):

Fustier, Céline. “Développement d'un réacteur intensifié en Carbure de Silicium pour la transposition en continu de réactions d'hydrosilylation : Development of Silicon Carbide equipments for the transposition of hydrosilylation reactions from batch to continuous.” 2012. Web. 28 Mar 2020.

Vancouver:

Fustier C. Développement d'un réacteur intensifié en Carbure de Silicium pour la transposition en continu de réactions d'hydrosilylation : Development of Silicon Carbide equipments for the transposition of hydrosilylation reactions from batch to continuous. [Internet] [Doctoral dissertation]. INP Toulouse; 2012. [cited 2020 Mar 28]. Available from: http://www.theses.fr/2012INPT0142.

Council of Science Editors:

Fustier C. Développement d'un réacteur intensifié en Carbure de Silicium pour la transposition en continu de réactions d'hydrosilylation : Development of Silicon Carbide equipments for the transposition of hydrosilylation reactions from batch to continuous. [Doctoral Dissertation]. INP Toulouse; 2012. Available from: http://www.theses.fr/2012INPT0142


Université Paris-Sud – Paris XI

17. Feghali, Elias. Nouveaux procédés catalytiques pour le recyclage de déchets ligno-cellulosiques, de polymères et de dérivés du CO₂ : New catalytic processes for the recycling of lignocellulosic waste, polymers and CO₂ derivatives.

Degree: Docteur es, Chimie, 2015, Université Paris-Sud – Paris XI

L’objectif de cette thèse était la mise au point de nouvelles méthodes de synthèse innovantes permettant le recyclage de déchets carbonés ou l’utilisation de matières… (more)

Subjects/Keywords: Dépolymérisation; Lignine; B(C6F5)3; Hydrosilylation; Recyclage de déchets; Biomasse; Depolymerization; Lignin; B(C6F5)3; Hydrosilylation; Waste recycling; Biomass

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APA (6th Edition):

Feghali, E. (2015). Nouveaux procédés catalytiques pour le recyclage de déchets ligno-cellulosiques, de polymères et de dérivés du CO₂ : New catalytic processes for the recycling of lignocellulosic waste, polymers and CO₂ derivatives. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2015PA112173

Chicago Manual of Style (16th Edition):

Feghali, Elias. “Nouveaux procédés catalytiques pour le recyclage de déchets ligno-cellulosiques, de polymères et de dérivés du CO₂ : New catalytic processes for the recycling of lignocellulosic waste, polymers and CO₂ derivatives.” 2015. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed March 28, 2020. http://www.theses.fr/2015PA112173.

MLA Handbook (7th Edition):

Feghali, Elias. “Nouveaux procédés catalytiques pour le recyclage de déchets ligno-cellulosiques, de polymères et de dérivés du CO₂ : New catalytic processes for the recycling of lignocellulosic waste, polymers and CO₂ derivatives.” 2015. Web. 28 Mar 2020.

Vancouver:

Feghali E. Nouveaux procédés catalytiques pour le recyclage de déchets ligno-cellulosiques, de polymères et de dérivés du CO₂ : New catalytic processes for the recycling of lignocellulosic waste, polymers and CO₂ derivatives. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2015. [cited 2020 Mar 28]. Available from: http://www.theses.fr/2015PA112173.

Council of Science Editors:

Feghali E. Nouveaux procédés catalytiques pour le recyclage de déchets ligno-cellulosiques, de polymères et de dérivés du CO₂ : New catalytic processes for the recycling of lignocellulosic waste, polymers and CO₂ derivatives. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2015. Available from: http://www.theses.fr/2015PA112173

18. Godou, Timothé. Mimer la chimie des hydrosilanes et hydroboranes par l’activation catalytique de dérivés silylés et borés de l’acide formique : Mimic the chemistry of hydrosilanes and hydroboranes by catalytic activation of silyl and boryl derivatives from formic acid.

Degree: Docteur es, Chimie, 2019, Université Paris-Saclay (ComUE)

Les besoins énergétiques mondiaux sont principalement satisfaits par l’utilisation de ressources fossiles telles que le pétrole, le charbon ou le gaz. L’utilisation de ces ressources… (more)

Subjects/Keywords: Co2; Catalyse homogène; Hydrosilylation; Hydroboration; Formiate de silicium; Formiate de bore; Co2; Homogenous catalysis; Hydrosilylation; Hydroboration; Silyl formate; Boryl formate

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APA (6th Edition):

Godou, T. (2019). Mimer la chimie des hydrosilanes et hydroboranes par l’activation catalytique de dérivés silylés et borés de l’acide formique : Mimic the chemistry of hydrosilanes and hydroboranes by catalytic activation of silyl and boryl derivatives from formic acid. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS307

Chicago Manual of Style (16th Edition):

Godou, Timothé. “Mimer la chimie des hydrosilanes et hydroboranes par l’activation catalytique de dérivés silylés et borés de l’acide formique : Mimic the chemistry of hydrosilanes and hydroboranes by catalytic activation of silyl and boryl derivatives from formic acid.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed March 28, 2020. http://www.theses.fr/2019SACLS307.

MLA Handbook (7th Edition):

Godou, Timothé. “Mimer la chimie des hydrosilanes et hydroboranes par l’activation catalytique de dérivés silylés et borés de l’acide formique : Mimic the chemistry of hydrosilanes and hydroboranes by catalytic activation of silyl and boryl derivatives from formic acid.” 2019. Web. 28 Mar 2020.

Vancouver:

Godou T. Mimer la chimie des hydrosilanes et hydroboranes par l’activation catalytique de dérivés silylés et borés de l’acide formique : Mimic the chemistry of hydrosilanes and hydroboranes by catalytic activation of silyl and boryl derivatives from formic acid. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Mar 28]. Available from: http://www.theses.fr/2019SACLS307.

Council of Science Editors:

Godou T. Mimer la chimie des hydrosilanes et hydroboranes par l’activation catalytique de dérivés silylés et borés de l’acide formique : Mimic the chemistry of hydrosilanes and hydroboranes by catalytic activation of silyl and boryl derivatives from formic acid. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS307


University of Alberta

19. Bunquin, Jeffrey. Empowering the Base Metals: Rational Design of Homogeneous Catalysts for Hydrotreatment, and Reduction of Organic Unsaturates.

Degree: PhD, Department of Chemistry, 2013, University of Alberta

 Hydrocarbon-soluble, low-coordinate, phosphoranimide-supported complexes of the base metals (iron, cobalt and nickel) were developed and evaluated for a range of stoichiometric and catalytic bond-forming and… (more)

Subjects/Keywords: Hydrosilylation; Cobalt; Hydrotreatment; Hydrodesulfurization; Phosphoranimide; Catalysis; Organometalics; Hydrogenation; Nickel

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APA (6th Edition):

Bunquin, J. (2013). Empowering the Base Metals: Rational Design of Homogeneous Catalysts for Hydrotreatment, and Reduction of Organic Unsaturates. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/zs25x874j

Chicago Manual of Style (16th Edition):

Bunquin, Jeffrey. “Empowering the Base Metals: Rational Design of Homogeneous Catalysts for Hydrotreatment, and Reduction of Organic Unsaturates.” 2013. Doctoral Dissertation, University of Alberta. Accessed March 28, 2020. https://era.library.ualberta.ca/files/zs25x874j.

MLA Handbook (7th Edition):

Bunquin, Jeffrey. “Empowering the Base Metals: Rational Design of Homogeneous Catalysts for Hydrotreatment, and Reduction of Organic Unsaturates.” 2013. Web. 28 Mar 2020.

Vancouver:

Bunquin J. Empowering the Base Metals: Rational Design of Homogeneous Catalysts for Hydrotreatment, and Reduction of Organic Unsaturates. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2020 Mar 28]. Available from: https://era.library.ualberta.ca/files/zs25x874j.

Council of Science Editors:

Bunquin J. Empowering the Base Metals: Rational Design of Homogeneous Catalysts for Hydrotreatment, and Reduction of Organic Unsaturates. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/zs25x874j

20. Hardy, Julie. Novel materials based on functionalised silsesquioxanes.

Degree: PhD, 2001, Open University

 The functionalisation of silsesquioxanes results in materials with novel physical properties. A series of compounds has been coupled with silsesquioxanes [HSiO3/2]8 and [SiO3/2]8 [OSi(CH3)2H]8 and… (more)

Subjects/Keywords: 541; Liquid crystals; Polyethers; Hydrosilylation

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APA (6th Edition):

Hardy, J. (2001). Novel materials based on functionalised silsesquioxanes. (Doctoral Dissertation). Open University. Retrieved from http://oro.open.ac.uk/19425/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343809

Chicago Manual of Style (16th Edition):

Hardy, Julie. “Novel materials based on functionalised silsesquioxanes.” 2001. Doctoral Dissertation, Open University. Accessed March 28, 2020. http://oro.open.ac.uk/19425/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343809.

MLA Handbook (7th Edition):

Hardy, Julie. “Novel materials based on functionalised silsesquioxanes.” 2001. Web. 28 Mar 2020.

Vancouver:

Hardy J. Novel materials based on functionalised silsesquioxanes. [Internet] [Doctoral dissertation]. Open University; 2001. [cited 2020 Mar 28]. Available from: http://oro.open.ac.uk/19425/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343809.

Council of Science Editors:

Hardy J. Novel materials based on functionalised silsesquioxanes. [Doctoral Dissertation]. Open University; 2001. Available from: http://oro.open.ac.uk/19425/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343809


Brock University

21. McLeod, Nicolas A. Synthesis, Catalysis and Stoichiometric Reactivity of Mo Imido Complexes .

Degree: Department of Chemistry, 2014, Brock University

 The syntheses, catalytic reactivity and mechanistic investigations of novel Mo(IV) and Mo(VI) imido systems is presented. Attempts at preparing mixed bis(imido) Mo(IV) complexes of the… (more)

Subjects/Keywords: Imido Chemistry; Agostic Bonding; Silanimine Complex; Hydrosilylation; Phosphine Cyclometallation

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APA (6th Edition):

McLeod, N. A. (2014). Synthesis, Catalysis and Stoichiometric Reactivity of Mo Imido Complexes . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/5435

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

McLeod, Nicolas A. “Synthesis, Catalysis and Stoichiometric Reactivity of Mo Imido Complexes .” 2014. Thesis, Brock University. Accessed March 28, 2020. http://hdl.handle.net/10464/5435.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

McLeod, Nicolas A. “Synthesis, Catalysis and Stoichiometric Reactivity of Mo Imido Complexes .” 2014. Web. 28 Mar 2020.

Vancouver:

McLeod NA. Synthesis, Catalysis and Stoichiometric Reactivity of Mo Imido Complexes . [Internet] [Thesis]. Brock University; 2014. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10464/5435.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

McLeod NA. Synthesis, Catalysis and Stoichiometric Reactivity of Mo Imido Complexes . [Thesis]. Brock University; 2014. Available from: http://hdl.handle.net/10464/5435

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Uniwersytet im. Adama Mickiewicza w Poznaniu

22. Dutkiewicz, Michał. Syntezy i nanotechnologie funkcjonalizowanych oktasilseskwioksanów .

Degree: 2011, Uniwersytet im. Adama Mickiewicza w Poznaniu

 Tematem niniejszej pracy jest synteza funkcjonalizowanych oktasilseskwioksanów (POSS) i zagadnienia związane z ich wykorzystaniem w technologiach wytwarzania nanokompozytów i materiałów hybrydowych. Jej główne cele to… (more)

Subjects/Keywords: Silseskwioksany; Silsesquioxanes; Hydrosililowanie; Hydrosilylation; Substytucja nukleofilowa; Nucleophilic substitution; Nanomateriały; Nanomaterials

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APA (6th Edition):

Dutkiewicz, M. (2011). Syntezy i nanotechnologie funkcjonalizowanych oktasilseskwioksanów . (Doctoral Dissertation). Uniwersytet im. Adama Mickiewicza w Poznaniu. Retrieved from http://hdl.handle.net/10593/1109

Chicago Manual of Style (16th Edition):

Dutkiewicz, Michał. “Syntezy i nanotechnologie funkcjonalizowanych oktasilseskwioksanów .” 2011. Doctoral Dissertation, Uniwersytet im. Adama Mickiewicza w Poznaniu. Accessed March 28, 2020. http://hdl.handle.net/10593/1109.

MLA Handbook (7th Edition):

Dutkiewicz, Michał. “Syntezy i nanotechnologie funkcjonalizowanych oktasilseskwioksanów .” 2011. Web. 28 Mar 2020.

Vancouver:

Dutkiewicz M. Syntezy i nanotechnologie funkcjonalizowanych oktasilseskwioksanów . [Internet] [Doctoral dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2011. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10593/1109.

Council of Science Editors:

Dutkiewicz M. Syntezy i nanotechnologie funkcjonalizowanych oktasilseskwioksanów . [Doctoral Dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2011. Available from: http://hdl.handle.net/10593/1109


NSYSU

23. Liao, Yi-Ting. Preparation of Flexible Organic/Inorganic Nanocomposites Based on Bifunctional Polyhedral Oligometric Silsesquioxanes.

Degree: Master, Materials and Optoelectronic Science, 2015, NSYSU

 In this study, two kinds of benzoxazine containing double-decker silsesquioxanes (DDSQ), Bz-DDSQ and PDMS-Bz-DDSQ were successfully synthesized by a combination of cycloaddition and hydrosilylation condensation.… (more)

Subjects/Keywords: Polybenzoxazines; Polydimethylsiloxane; Hydrosilylation condensation; Polyhedral Oligomeric Silsesquioxanes; Double-decker silsesquioxanes

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APA (6th Edition):

Liao, Y. (2015). Preparation of Flexible Organic/Inorganic Nanocomposites Based on Bifunctional Polyhedral Oligometric Silsesquioxanes. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0603115-145424

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Liao, Yi-Ting. “Preparation of Flexible Organic/Inorganic Nanocomposites Based on Bifunctional Polyhedral Oligometric Silsesquioxanes.” 2015. Thesis, NSYSU. Accessed March 28, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0603115-145424.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Liao, Yi-Ting. “Preparation of Flexible Organic/Inorganic Nanocomposites Based on Bifunctional Polyhedral Oligometric Silsesquioxanes.” 2015. Web. 28 Mar 2020.

Vancouver:

Liao Y. Preparation of Flexible Organic/Inorganic Nanocomposites Based on Bifunctional Polyhedral Oligometric Silsesquioxanes. [Internet] [Thesis]. NSYSU; 2015. [cited 2020 Mar 28]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0603115-145424.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Liao Y. Preparation of Flexible Organic/Inorganic Nanocomposites Based on Bifunctional Polyhedral Oligometric Silsesquioxanes. [Thesis]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0603115-145424

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Toledo

24. Tafazolian, Hosein. Hydroamination and Hydrosilylation Catalyzed by Cationic Palladium- and Nickel(allyl) Complexes Supported by 3-Iminophosphine Ligands.

Degree: PhD, Chemistry, 2016, University of Toledo

 Chapter 1. A brief introduction to organometallic chemistry and catalysis is presented to explain the basics of the field to the reader. A few examples… (more)

Subjects/Keywords: Chemistry; Hydroamination; hydrosilylation; palladium; nickel; 3-iminophosphine ligands

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APA (6th Edition):

Tafazolian, H. (2016). Hydroamination and Hydrosilylation Catalyzed by Cationic Palladium- and Nickel(allyl) Complexes Supported by 3-Iminophosphine Ligands. (Doctoral Dissertation). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1473397460390363

Chicago Manual of Style (16th Edition):

Tafazolian, Hosein. “Hydroamination and Hydrosilylation Catalyzed by Cationic Palladium- and Nickel(allyl) Complexes Supported by 3-Iminophosphine Ligands.” 2016. Doctoral Dissertation, University of Toledo. Accessed March 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1473397460390363.

MLA Handbook (7th Edition):

Tafazolian, Hosein. “Hydroamination and Hydrosilylation Catalyzed by Cationic Palladium- and Nickel(allyl) Complexes Supported by 3-Iminophosphine Ligands.” 2016. Web. 28 Mar 2020.

Vancouver:

Tafazolian H. Hydroamination and Hydrosilylation Catalyzed by Cationic Palladium- and Nickel(allyl) Complexes Supported by 3-Iminophosphine Ligands. [Internet] [Doctoral dissertation]. University of Toledo; 2016. [cited 2020 Mar 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1473397460390363.

Council of Science Editors:

Tafazolian H. Hydroamination and Hydrosilylation Catalyzed by Cationic Palladium- and Nickel(allyl) Complexes Supported by 3-Iminophosphine Ligands. [Doctoral Dissertation]. University of Toledo; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1473397460390363


Uniwersytet im. Adama Mickiewicza w Poznaniu

25. Franczyk, Adrian. Mono- i dwufunkcyjne silseskwioksany – synteza i zastosowanie w kompozytach polimerowych .

Degree: 2014, Uniwersytet im. Adama Mickiewicza w Poznaniu

 Praca doktorska dotyczyła opracowania metod syntezy mono- (T8R7R’) i dwufunkcyjnych (Ph8Si10O14(SiRR’)2) silseskwioksanów oraz ich zastosowania w syntezie polimerów hybrydowych. W pierwszym etapie prac na drodze… (more)

Subjects/Keywords: Silseskwioksany; Silsesquioxanes; Hydrosililowanie; Hydrosilylation; ATRP; Polimetakrylany; Polymethacrylates; Hybrydy; Hybrids

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APA (6th Edition):

Franczyk, A. (2014). Mono- i dwufunkcyjne silseskwioksany – synteza i zastosowanie w kompozytach polimerowych . (Doctoral Dissertation). Uniwersytet im. Adama Mickiewicza w Poznaniu. Retrieved from http://hdl.handle.net/10593/11475

Chicago Manual of Style (16th Edition):

Franczyk, Adrian. “Mono- i dwufunkcyjne silseskwioksany – synteza i zastosowanie w kompozytach polimerowych .” 2014. Doctoral Dissertation, Uniwersytet im. Adama Mickiewicza w Poznaniu. Accessed March 28, 2020. http://hdl.handle.net/10593/11475.

MLA Handbook (7th Edition):

Franczyk, Adrian. “Mono- i dwufunkcyjne silseskwioksany – synteza i zastosowanie w kompozytach polimerowych .” 2014. Web. 28 Mar 2020.

Vancouver:

Franczyk A. Mono- i dwufunkcyjne silseskwioksany – synteza i zastosowanie w kompozytach polimerowych . [Internet] [Doctoral dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2014. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10593/11475.

Council of Science Editors:

Franczyk A. Mono- i dwufunkcyjne silseskwioksany – synteza i zastosowanie w kompozytach polimerowych . [Doctoral Dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2014. Available from: http://hdl.handle.net/10593/11475

26. Parker, Sarah Elizabeth. 1,2-Selective Hydrosilylation of Conjugated Dienes.

Degree: PhD, Chemistry and Chemical Biology, 2014, Harvard University

Selective 1,2-hydrosilylation of 1,3-dienes is a challenging problem to solve for transition metal catalysis. Butadiene, specifically, would be a useful substrate because 3-butenylsilane products have… (more)

Subjects/Keywords: Chemistry; Catalysis; Hydrosilylation; Platinum

…Selective Hydrosilylation .......................................................... 81 Figure 4… …Hydrosilylation of Butadiene....................... 97 Figure 7. Optimized structures for the products… …175 Figure 13. Hydrosilylation Timecourse Using Precatalyst 32… …177 Figure 14. Hydrosilylation Timecourse Using Precatalyst 37… …179 Figure 15. Hydrosilylation Timecourse Using Precatalyst 16… 

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

APA (6th Edition):

Parker, S. E. (2014). 1,2-Selective Hydrosilylation of Conjugated Dienes. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274560

Chicago Manual of Style (16th Edition):

Parker, Sarah Elizabeth. “1,2-Selective Hydrosilylation of Conjugated Dienes.” 2014. Doctoral Dissertation, Harvard University. Accessed March 28, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274560.

MLA Handbook (7th Edition):

Parker, Sarah Elizabeth. “1,2-Selective Hydrosilylation of Conjugated Dienes.” 2014. Web. 28 Mar 2020.

Vancouver:

Parker SE. 1,2-Selective Hydrosilylation of Conjugated Dienes. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2020 Mar 28]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274560.

Council of Science Editors:

Parker SE. 1,2-Selective Hydrosilylation of Conjugated Dienes. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274560


Oklahoma State University

27. Kwaramba, Farai Brian. Development and Design of Nanomaterial Reagents in Conjunction with New Methods for Their Synthetic Applications.

Degree: Chemistry, 2014, Oklahoma State University

 This Ph.D. deals with the integration of nanotechnology with organometallic/ organic synthetic technologies. The first part of this research sought to develop a library of… (more)

Subjects/Keywords: alkynyl-silanes; hydrosilylation; iridium catalysis; metal-nanoparticle catalysts; molecular-gears; nanofabrication

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APA (6th Edition):

Kwaramba, F. B. (2014). Development and Design of Nanomaterial Reagents in Conjunction with New Methods for Their Synthetic Applications. (Thesis). Oklahoma State University. Retrieved from http://hdl.handle.net/11244/14949

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kwaramba, Farai Brian. “Development and Design of Nanomaterial Reagents in Conjunction with New Methods for Their Synthetic Applications.” 2014. Thesis, Oklahoma State University. Accessed March 28, 2020. http://hdl.handle.net/11244/14949.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kwaramba, Farai Brian. “Development and Design of Nanomaterial Reagents in Conjunction with New Methods for Their Synthetic Applications.” 2014. Web. 28 Mar 2020.

Vancouver:

Kwaramba FB. Development and Design of Nanomaterial Reagents in Conjunction with New Methods for Their Synthetic Applications. [Internet] [Thesis]. Oklahoma State University; 2014. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/11244/14949.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kwaramba FB. Development and Design of Nanomaterial Reagents in Conjunction with New Methods for Their Synthetic Applications. [Thesis]. Oklahoma State University; 2014. Available from: http://hdl.handle.net/11244/14949

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université Catholique de Louvain

28. Gathy, Thomas. Etude théorique des réactions d'hydrosilylation des cétones par un catalyseur cuivre-diphosphine.

Degree: 2012, Université Catholique de Louvain

This work consists in a theoretical study of the hydrosilylation reactions of ketones by a copper-diphosphine catalyst. The active species in these systems is a… (more)

Subjects/Keywords: Hydrosilylation; Copper catalyst; Catalytic cycle; Theoretical study; DFT

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APA (6th Edition):

Gathy, T. (2012). Etude théorique des réactions d'hydrosilylation des cétones par un catalyseur cuivre-diphosphine. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/118666

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gathy, Thomas. “Etude théorique des réactions d'hydrosilylation des cétones par un catalyseur cuivre-diphosphine.” 2012. Thesis, Université Catholique de Louvain. Accessed March 28, 2020. http://hdl.handle.net/2078.1/118666.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gathy, Thomas. “Etude théorique des réactions d'hydrosilylation des cétones par un catalyseur cuivre-diphosphine.” 2012. Web. 28 Mar 2020.

Vancouver:

Gathy T. Etude théorique des réactions d'hydrosilylation des cétones par un catalyseur cuivre-diphosphine. [Internet] [Thesis]. Université Catholique de Louvain; 2012. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/2078.1/118666.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gathy T. Etude théorique des réactions d'hydrosilylation des cétones par un catalyseur cuivre-diphosphine. [Thesis]. Université Catholique de Louvain; 2012. Available from: http://hdl.handle.net/2078.1/118666

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Columbia University

29. Ruccolo, Serge Michel. Zinc Supported by Nitrogen-Rich Ligands: Applications Towards Catalytic Hydrosilylation And Modeling Zinc Enzymes.

Degree: 2016, Columbia University

 In chapter 1, I discuss how ligand architecture in tripodal nitrogen-rich ligands can drastically affect the structure of zinc complexes featuring these ligands. The synthesis… (more)

Subjects/Keywords: Ligand binding (Biochemistry); Ligands; Hydrosilylation; Zinc enzymes; Chemistry; Zinc

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

APA (6th Edition):

Ruccolo, S. M. (2016). Zinc Supported by Nitrogen-Rich Ligands: Applications Towards Catalytic Hydrosilylation And Modeling Zinc Enzymes. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8222V0F

Chicago Manual of Style (16th Edition):

Ruccolo, Serge Michel. “Zinc Supported by Nitrogen-Rich Ligands: Applications Towards Catalytic Hydrosilylation And Modeling Zinc Enzymes.” 2016. Doctoral Dissertation, Columbia University. Accessed March 28, 2020. https://doi.org/10.7916/D8222V0F.

MLA Handbook (7th Edition):

Ruccolo, Serge Michel. “Zinc Supported by Nitrogen-Rich Ligands: Applications Towards Catalytic Hydrosilylation And Modeling Zinc Enzymes.” 2016. Web. 28 Mar 2020.

Vancouver:

Ruccolo SM. Zinc Supported by Nitrogen-Rich Ligands: Applications Towards Catalytic Hydrosilylation And Modeling Zinc Enzymes. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2020 Mar 28]. Available from: https://doi.org/10.7916/D8222V0F.

Council of Science Editors:

Ruccolo SM. Zinc Supported by Nitrogen-Rich Ligands: Applications Towards Catalytic Hydrosilylation And Modeling Zinc Enzymes. [Doctoral Dissertation]. Columbia University; 2016. Available from: https://doi.org/10.7916/D8222V0F


University of Toronto

30. LIU, JIA BAO. Hydrosilylation of Ketones Catalyzed by Reactive Fe and Co Complexes Constructed from Isolated Picolyl-Functionalized N-Heterocyclic Carbenes.

Degree: 2018, University of Toronto

Silanes are commonly used reducing agents due to their reactive nature and the high earth-abundance of silicon. Many metal complexes are known to catalyze the… (more)

Subjects/Keywords: free picolyl-functionalized N-heterocyclic carbenes; hydrosilylation of ketones; polymethylhydrosiloxane; 0488

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

APA (6th Edition):

LIU, J. B. (2018). Hydrosilylation of Ketones Catalyzed by Reactive Fe and Co Complexes Constructed from Isolated Picolyl-Functionalized N-Heterocyclic Carbenes. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91561

Chicago Manual of Style (16th Edition):

LIU, JIA BAO. “Hydrosilylation of Ketones Catalyzed by Reactive Fe and Co Complexes Constructed from Isolated Picolyl-Functionalized N-Heterocyclic Carbenes.” 2018. Masters Thesis, University of Toronto. Accessed March 28, 2020. http://hdl.handle.net/1807/91561.

MLA Handbook (7th Edition):

LIU, JIA BAO. “Hydrosilylation of Ketones Catalyzed by Reactive Fe and Co Complexes Constructed from Isolated Picolyl-Functionalized N-Heterocyclic Carbenes.” 2018. Web. 28 Mar 2020.

Vancouver:

LIU JB. Hydrosilylation of Ketones Catalyzed by Reactive Fe and Co Complexes Constructed from Isolated Picolyl-Functionalized N-Heterocyclic Carbenes. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/1807/91561.

Council of Science Editors:

LIU JB. Hydrosilylation of Ketones Catalyzed by Reactive Fe and Co Complexes Constructed from Isolated Picolyl-Functionalized N-Heterocyclic Carbenes. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91561

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