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You searched for subject:(N Heterocyclic Carbene). Showing records 91 – 113 of 113 total matches.

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91. GUO SHUAI. PALLADIUM, GOLD AND COPPER CHEMISTRY OF N-HETEROCYCLIC CARBENES.

Degree: 2014, National University of Singapore

Subjects/Keywords: N-heterocyclic carbene; palladium; gold; copper; donating ability; homogenous catalysis

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

APA (6th Edition):

SHUAI, G. (2014). PALLADIUM, GOLD AND COPPER CHEMISTRY OF N-HETEROCYCLIC CARBENES. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/119262

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):

SHUAI, GUO. “PALLADIUM, GOLD AND COPPER CHEMISTRY OF N-HETEROCYCLIC CARBENES.” 2014. Thesis, National University of Singapore. Accessed October 18, 2019. http://scholarbank.nus.edu.sg/handle/10635/119262.

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

MLA Handbook (7th Edition):

SHUAI, GUO. “PALLADIUM, GOLD AND COPPER CHEMISTRY OF N-HETEROCYCLIC CARBENES.” 2014. Web. 18 Oct 2019.

Vancouver:

SHUAI G. PALLADIUM, GOLD AND COPPER CHEMISTRY OF N-HETEROCYCLIC CARBENES. [Internet] [Thesis]. National University of Singapore; 2014. [cited 2019 Oct 18]. Available from: http://scholarbank.nus.edu.sg/handle/10635/119262.

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

Council of Science Editors:

SHUAI G. PALLADIUM, GOLD AND COPPER CHEMISTRY OF N-HETEROCYCLIC CARBENES. [Thesis]. National University of Singapore; 2014. Available from: http://scholarbank.nus.edu.sg/handle/10635/119262

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


Queens University

92. Li, Zhijun. Self-Assembled N-Heterocyclic Carbene Monolayers on Gold as a Tunable Platform for Designing Biosensor Surfaces .

Degree: Chemistry, Queens University

 Surface plasmon resonance (SPR)-based biosensing is an excellent tool to probe the recognition process between biomolecules in real-time, without need for labels. Thiol-based self-assembled monolayers… (more)

Subjects/Keywords: Self-assembled monolayer; N-heterocyclic carbene monolayer; Biosensor surface; Surface plasmon resonance

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APA (6th Edition):

Li, Z. (n.d.). Self-Assembled N-Heterocyclic Carbene Monolayers on Gold as a Tunable Platform for Designing Biosensor Surfaces . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/15899

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Li, Zhijun. “Self-Assembled N-Heterocyclic Carbene Monolayers on Gold as a Tunable Platform for Designing Biosensor Surfaces .” Thesis, Queens University. Accessed October 18, 2019. http://hdl.handle.net/1974/15899.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Li, Zhijun. “Self-Assembled N-Heterocyclic Carbene Monolayers on Gold as a Tunable Platform for Designing Biosensor Surfaces .” Web. 18 Oct 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Li Z. Self-Assembled N-Heterocyclic Carbene Monolayers on Gold as a Tunable Platform for Designing Biosensor Surfaces . [Internet] [Thesis]. Queens University; [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1974/15899.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Li Z. Self-Assembled N-Heterocyclic Carbene Monolayers on Gold as a Tunable Platform for Designing Biosensor Surfaces . [Thesis]. Queens University; Available from: http://hdl.handle.net/1974/15899

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Colorado State University

93. Dunn, Eric F. Investigation into discrete molecular catalysts for biomass conversion into 5-hydroxymethylfurfural.

Degree: MS(M.S.), Chemistry, 2007, Colorado State University

 As part of ongoing research into the conversion of biomass into the platform chemical 5-hydroxymethylfurfural (HMF), two primary investigations have been performed. The first is… (more)

Subjects/Keywords: 5-hydroxymethylfurfural; biomass; chromium; glucose; Ionic liquids; N-heterocyclic carbene

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APA (6th Edition):

Dunn, E. F. (2007). Investigation into discrete molecular catalysts for biomass conversion into 5-hydroxymethylfurfural. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/80234

Chicago Manual of Style (16th Edition):

Dunn, Eric F. “Investigation into discrete molecular catalysts for biomass conversion into 5-hydroxymethylfurfural.” 2007. Masters Thesis, Colorado State University. Accessed October 18, 2019. http://hdl.handle.net/10217/80234.

MLA Handbook (7th Edition):

Dunn, Eric F. “Investigation into discrete molecular catalysts for biomass conversion into 5-hydroxymethylfurfural.” 2007. Web. 18 Oct 2019.

Vancouver:

Dunn EF. Investigation into discrete molecular catalysts for biomass conversion into 5-hydroxymethylfurfural. [Internet] [Masters thesis]. Colorado State University; 2007. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10217/80234.

Council of Science Editors:

Dunn EF. Investigation into discrete molecular catalysts for biomass conversion into 5-hydroxymethylfurfural. [Masters Thesis]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/80234

94. Mejuto Nieblas, Carmen. Poly-N-Heterocyclic Carbene Ligands with Polyaromatic Linkers. Self-Assembly and Host-Guest Chemistry.

Degree: 2017, Universitat Jaume I

 En esta Tesis Doctoral se ha sintetizado una serie de ligandos politópicos basados en ligandos NHC y MIC mediante diferentes rutas sintéticas que dieron lugar… (more)

Subjects/Keywords: N-Heterocyclic Carbene Ligands; Self-Assembly; Host-Guest Chemistry; Mesoionic Carbene Ligands; Catalysis; Polyaromatic; Química; 546

n-butyl NaHMDS Sodium bis(trimethyl)silylamide NHC N-heterocyclic carbene… …MeOH Methanol MeCN Acetonitrile Mes 2,4,6-trimethylphenyl MIC Mesoionic carbene nBu… …síntesis de metalo-estructuras poliaromáticas basadas en carbenos poli-N-heterocíclicos (… …para la tesis, tales como el autoensamblaje o carbenos N-heterocíclicos. También se incluye… …carbenos N-heterocíclicos (NHCs) y carbenos mesoiónicos (MICs), y fueron… 

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APA (6th Edition):

Mejuto Nieblas, C. (2017). Poly-N-Heterocyclic Carbene Ligands with Polyaromatic Linkers. Self-Assembly and Host-Guest Chemistry. (Thesis). Universitat Jaume I. Retrieved from http://hdl.handle.net/10803/404306

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):

Mejuto Nieblas, Carmen. “Poly-N-Heterocyclic Carbene Ligands with Polyaromatic Linkers. Self-Assembly and Host-Guest Chemistry.” 2017. Thesis, Universitat Jaume I. Accessed October 18, 2019. http://hdl.handle.net/10803/404306.

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

MLA Handbook (7th Edition):

Mejuto Nieblas, Carmen. “Poly-N-Heterocyclic Carbene Ligands with Polyaromatic Linkers. Self-Assembly and Host-Guest Chemistry.” 2017. Web. 18 Oct 2019.

Vancouver:

Mejuto Nieblas C. Poly-N-Heterocyclic Carbene Ligands with Polyaromatic Linkers. Self-Assembly and Host-Guest Chemistry. [Internet] [Thesis]. Universitat Jaume I; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10803/404306.

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

Council of Science Editors:

Mejuto Nieblas C. Poly-N-Heterocyclic Carbene Ligands with Polyaromatic Linkers. Self-Assembly and Host-Guest Chemistry. [Thesis]. Universitat Jaume I; 2017. Available from: http://hdl.handle.net/10803/404306

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

95. YUAN DAN. GROUP 10 TRANSITION METAL CHEMISTRY OF SULFUR-FUNCTIONALIZED/NON-CLASSICAL N-HETEROCYCLIC CARBENE LIGANDS.

Degree: 2011, National University of Singapore

Subjects/Keywords: N-heterocyclic carbene ligands; transition metal; sulfur-function; non-classical carbene; catalysis; donor strength

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APA (6th Edition):

DAN, Y. (2011). GROUP 10 TRANSITION METAL CHEMISTRY OF SULFUR-FUNCTIONALIZED/NON-CLASSICAL N-HETEROCYCLIC CARBENE LIGANDS. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/30784

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):

DAN, YUAN. “GROUP 10 TRANSITION METAL CHEMISTRY OF SULFUR-FUNCTIONALIZED/NON-CLASSICAL N-HETEROCYCLIC CARBENE LIGANDS.” 2011. Thesis, National University of Singapore. Accessed October 18, 2019. http://scholarbank.nus.edu.sg/handle/10635/30784.

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

MLA Handbook (7th Edition):

DAN, YUAN. “GROUP 10 TRANSITION METAL CHEMISTRY OF SULFUR-FUNCTIONALIZED/NON-CLASSICAL N-HETEROCYCLIC CARBENE LIGANDS.” 2011. Web. 18 Oct 2019.

Vancouver:

DAN Y. GROUP 10 TRANSITION METAL CHEMISTRY OF SULFUR-FUNCTIONALIZED/NON-CLASSICAL N-HETEROCYCLIC CARBENE LIGANDS. [Internet] [Thesis]. National University of Singapore; 2011. [cited 2019 Oct 18]. Available from: http://scholarbank.nus.edu.sg/handle/10635/30784.

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

Council of Science Editors:

DAN Y. GROUP 10 TRANSITION METAL CHEMISTRY OF SULFUR-FUNCTIONALIZED/NON-CLASSICAL N-HETEROCYCLIC CARBENE LIGANDS. [Thesis]. National University of Singapore; 2011. Available from: http://scholarbank.nus.edu.sg/handle/10635/30784

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

96. Schnee, Gilles. Synthèse et réactivité de nouveaux complexes des métaux du groupe 13 portés par des ligands carbènes N-hétérocycliques : Synthesis and reactivity of group 13 metals complexes supported by N-heterocyclic carbenes.

Degree: Docteur es, Chimie, 2012, Université de Strasbourg

Au début de ces travaux, peu d’études avaient été faites sur la complexation des carbènes N-hétérocycliques avec des métaux oxophiles, électropositifs et à hauts degrés… (more)

Subjects/Keywords: Chimie organométallique; Métaux du groupe 13; Carbène N-hétérocyclique (NHC); Complexe NHC anormaux; Complexe mésoionique; Complexes dicarbènes N-hétérocycliques (NHDCs); Paires de Lewis frustrées (FLPs); Réactif de Tebbe; Organometallic chemistry; Group 13 metals; N-heterocyclic carbene (NHC); Abnormal NHC complexes; Frustrated Lewis Pairs (FLPs); N-heterocyclic dicarbenes (NHDCs); Tebbe reagent; 547.2; 547.7

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APA (6th Edition):

Schnee, G. (2012). Synthèse et réactivité de nouveaux complexes des métaux du groupe 13 portés par des ligands carbènes N-hétérocycliques : Synthesis and reactivity of group 13 metals complexes supported by N-heterocyclic carbenes. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAF053

Chicago Manual of Style (16th Edition):

Schnee, Gilles. “Synthèse et réactivité de nouveaux complexes des métaux du groupe 13 portés par des ligands carbènes N-hétérocycliques : Synthesis and reactivity of group 13 metals complexes supported by N-heterocyclic carbenes.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed October 18, 2019. http://www.theses.fr/2012STRAF053.

MLA Handbook (7th Edition):

Schnee, Gilles. “Synthèse et réactivité de nouveaux complexes des métaux du groupe 13 portés par des ligands carbènes N-hétérocycliques : Synthesis and reactivity of group 13 metals complexes supported by N-heterocyclic carbenes.” 2012. Web. 18 Oct 2019.

Vancouver:

Schnee G. Synthèse et réactivité de nouveaux complexes des métaux du groupe 13 portés par des ligands carbènes N-hétérocycliques : Synthesis and reactivity of group 13 metals complexes supported by N-heterocyclic carbenes. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2012STRAF053.

Council of Science Editors:

Schnee G. Synthèse et réactivité de nouveaux complexes des métaux du groupe 13 portés par des ligands carbènes N-hétérocycliques : Synthesis and reactivity of group 13 metals complexes supported by N-heterocyclic carbenes. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAF053

97. Dahm, Georges. Metallocarbenes for therapeutic applications : Métallocarbènes pour des applications thérapeutiques.

Degree: Docteur es, Chimie, 2014, Université de Strasbourg

Les complexes métalliques des carbènes N-hétérocycliques (NHC) présentent un grand potentiel comme anticancéreux. En particulier, des études in vitro ont confirmés une cytotoxicité supérieure au… (more)

Subjects/Keywords: Complexes NHC (carbènes N-hétérocycliques); Complexes de platine; Médicaments anticancéreux; Post-fonctionnalisation; Polyethylenimine; Cytotoxicité; Tests in vivo; Chimie organométallique; N-Heterocyclic carbene (NHC) complexes; Platinum complexes; Anticancer drugs; Post-synthetic functionalization; Polyethylenimine; Cytotoxicity; In vivo tests; Organometallic chemistry; 547.2

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APA (6th Edition):

Dahm, G. (2014). Metallocarbenes for therapeutic applications : Métallocarbènes pour des applications thérapeutiques. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2014STRAE037

Chicago Manual of Style (16th Edition):

Dahm, Georges. “Metallocarbenes for therapeutic applications : Métallocarbènes pour des applications thérapeutiques.” 2014. Doctoral Dissertation, Université de Strasbourg. Accessed October 18, 2019. http://www.theses.fr/2014STRAE037.

MLA Handbook (7th Edition):

Dahm, Georges. “Metallocarbenes for therapeutic applications : Métallocarbènes pour des applications thérapeutiques.” 2014. Web. 18 Oct 2019.

Vancouver:

Dahm G. Metallocarbenes for therapeutic applications : Métallocarbènes pour des applications thérapeutiques. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2014. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2014STRAE037.

Council of Science Editors:

Dahm G. Metallocarbenes for therapeutic applications : Métallocarbènes pour des applications thérapeutiques. [Doctoral Dissertation]. Université de Strasbourg; 2014. Available from: http://www.theses.fr/2014STRAE037

98. Zheng, Jianxia. Earth-abundant metal complexes for catalyzed hydroelementation : Réactions d’hydroélémentation catalysées par des complexes des métaux de transition abondants.

Degree: Docteur es, Chimie, 2014, Rennes 1

Ce travail de recherche est consacré au développement de catalyseurs à base de métaux de transition abondants de la première rangée du tableau périodique, tels… (more)

Subjects/Keywords: Hydrosilylation; Amination réductrice; Hydroboration; Méthylation; Cyclométallation; Carbène N-Hétérocyclique; Composés carbonylés; Acides carboxyliques; Dioxyde de carbone; Nickel; Manganèse; Fer; Hydrosilylation; Reductive amination; Hydroboration; Methylation; Cyclometalation; N-Heterocyclic carbene; Carbonyl compounds; Carboxylic acids; Carbon dioxide; Nickel; Manganese; Iron

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APA (6th Edition):

Zheng, J. (2014). Earth-abundant metal complexes for catalyzed hydroelementation : Réactions d’hydroélémentation catalysées par des complexes des métaux de transition abondants. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2014REN1S148

Chicago Manual of Style (16th Edition):

Zheng, Jianxia. “Earth-abundant metal complexes for catalyzed hydroelementation : Réactions d’hydroélémentation catalysées par des complexes des métaux de transition abondants.” 2014. Doctoral Dissertation, Rennes 1. Accessed October 18, 2019. http://www.theses.fr/2014REN1S148.

MLA Handbook (7th Edition):

Zheng, Jianxia. “Earth-abundant metal complexes for catalyzed hydroelementation : Réactions d’hydroélémentation catalysées par des complexes des métaux de transition abondants.” 2014. Web. 18 Oct 2019.

Vancouver:

Zheng J. Earth-abundant metal complexes for catalyzed hydroelementation : Réactions d’hydroélémentation catalysées par des complexes des métaux de transition abondants. [Internet] [Doctoral dissertation]. Rennes 1; 2014. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2014REN1S148.

Council of Science Editors:

Zheng J. Earth-abundant metal complexes for catalyzed hydroelementation : Réactions d’hydroélémentation catalysées par des complexes des métaux de transition abondants. [Doctoral Dissertation]. Rennes 1; 2014. Available from: http://www.theses.fr/2014REN1S148


University of Akron

99. Melaiye, Abdulkareem M. Synthesis and Antimicrobial Properties of Silver(I) N-Heterocyclic Carbene Complexes.

Degree: PhD, Chemistry, 2005, University of Akron

  New symmetric and asymmetric types of N-heterocyclic carbene (NHC) precursors, grouped into mono-dentate, bi-dentate and tri-dentate chelating ligands, were synthesized. The reaction of the… (more)

Subjects/Keywords: Silver(I); N-heterocyclic carbenes; Antimicrobial; Electrospinning; Nanosilver ions; Nanofiber mat; Silver(I)N-heterocyclic carbene complexes; Bactericidal; fungicidal; Electrospun fiber mat

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APA (6th Edition):

Melaiye, A. M. (2005). Synthesis and Antimicrobial Properties of Silver(I) N-Heterocyclic Carbene Complexes. (Doctoral Dissertation). University of Akron. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=akron1124310734

Chicago Manual of Style (16th Edition):

Melaiye, Abdulkareem M. “Synthesis and Antimicrobial Properties of Silver(I) N-Heterocyclic Carbene Complexes.” 2005. Doctoral Dissertation, University of Akron. Accessed October 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1124310734.

MLA Handbook (7th Edition):

Melaiye, Abdulkareem M. “Synthesis and Antimicrobial Properties of Silver(I) N-Heterocyclic Carbene Complexes.” 2005. Web. 18 Oct 2019.

Vancouver:

Melaiye AM. Synthesis and Antimicrobial Properties of Silver(I) N-Heterocyclic Carbene Complexes. [Internet] [Doctoral dissertation]. University of Akron; 2005. [cited 2019 Oct 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1124310734.

Council of Science Editors:

Melaiye AM. Synthesis and Antimicrobial Properties of Silver(I) N-Heterocyclic Carbene Complexes. [Doctoral Dissertation]. University of Akron; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1124310734

100. Price, Jacquelyn T. Novel Thiophene Supported N,N'-Chelating Ligands and Their Main Group Compounds.

Degree: 2013, University of Western Ontario

 Main group chemistry has advanced from studying fundamental curiosities, including low oxidation state, low-valent, p-block elements to tailoring these unique, reactive species for specific functional… (more)

Subjects/Keywords: Thiophene; photochromic; dithienylethene; pnictogen; N-heterocyclic carbene; N-heterocyclic phosphenium; low coordinate; main group chemistry; Inorganic Chemistry; Materials Chemistry

…structures of the N-heterocyclic carbene............................................3 Figure 1.3… …carbene N-heterocyclic phosphenium N-heterocyclic pnictene nanometer n-methylmorpholine nuclear… …Figure 1.2: Resonance structures of the N-heterocyclic carbene. NHCs share many similarities… …of NO+. In contrast to NHPs, N-heterocyclic carbene metal complexes are known with almost… …minute(s) milliliter millimole molecular weight mole n-butyllithium N-heterocyclic… 

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APA (6th Edition):

Price, J. T. (2013). Novel Thiophene Supported N,N'-Chelating Ligands and Their Main Group Compounds. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1304

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):

Price, Jacquelyn T. “Novel Thiophene Supported N,N'-Chelating Ligands and Their Main Group Compounds.” 2013. Thesis, University of Western Ontario. Accessed October 18, 2019. https://ir.lib.uwo.ca/etd/1304.

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

MLA Handbook (7th Edition):

Price, Jacquelyn T. “Novel Thiophene Supported N,N'-Chelating Ligands and Their Main Group Compounds.” 2013. Web. 18 Oct 2019.

Vancouver:

Price JT. Novel Thiophene Supported N,N'-Chelating Ligands and Their Main Group Compounds. [Internet] [Thesis]. University of Western Ontario; 2013. [cited 2019 Oct 18]. Available from: https://ir.lib.uwo.ca/etd/1304.

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

Council of Science Editors:

Price JT. Novel Thiophene Supported N,N'-Chelating Ligands and Their Main Group Compounds. [Thesis]. University of Western Ontario; 2013. Available from: https://ir.lib.uwo.ca/etd/1304

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


University of Alberta

101. Momeni Taheri, Mohammad Reza. Computational Investigations on Excited State Properties of Cyanine Dyes and Carbene-bound Main Group Elements.

Degree: PhD, Department of Chemistry, 2015, University of Alberta

 The first section of this thesis is concerned with the computational study of excited state properties of boron-dipyrromethene (BODIPY) organic dyes using ab initio and… (more)

Subjects/Keywords: Excited State Properties; Bonding Properties; Density Functional Theory; Time Dependent Density Functional Theory; Natural Bond Orbital; Cyanine Dyes; Carbene; Inorganic Complexes; Boron Nitride Compounds; Boron dipyrromethene; BODIPY; CASSCF; CASPT2; Coupled Cluster Methods; Benchmark Study; Photodynamic Therapy; Nanochemistry; Germanium Nanocrystals; Atoms in Molecules; Electronic Structure Methods; Borane and Silane Compounds; Vertical Excitation Energies; Adiabatic Excitation Energies; Complexation Energies; Bond Dissociation Energies; N-heterocyclic Carbene; N-heterocyclic Olefine; Aminoalkyl Carbenes; Energy Decomposition Analysis; Theoretical Chemistry; Computational Chemistry

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APA (6th Edition):

Momeni Taheri, M. R. (2015). Computational Investigations on Excited State Properties of Cyanine Dyes and Carbene-bound Main Group Elements. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/csj139212h

Chicago Manual of Style (16th Edition):

Momeni Taheri, Mohammad Reza. “Computational Investigations on Excited State Properties of Cyanine Dyes and Carbene-bound Main Group Elements.” 2015. Doctoral Dissertation, University of Alberta. Accessed October 18, 2019. https://era.library.ualberta.ca/files/csj139212h.

MLA Handbook (7th Edition):

Momeni Taheri, Mohammad Reza. “Computational Investigations on Excited State Properties of Cyanine Dyes and Carbene-bound Main Group Elements.” 2015. Web. 18 Oct 2019.

Vancouver:

Momeni Taheri MR. Computational Investigations on Excited State Properties of Cyanine Dyes and Carbene-bound Main Group Elements. [Internet] [Doctoral dissertation]. University of Alberta; 2015. [cited 2019 Oct 18]. Available from: https://era.library.ualberta.ca/files/csj139212h.

Council of Science Editors:

Momeni Taheri MR. Computational Investigations on Excited State Properties of Cyanine Dyes and Carbene-bound Main Group Elements. [Doctoral Dissertation]. University of Alberta; 2015. Available from: https://era.library.ualberta.ca/files/csj139212h


University of Western Australia

102. Brayshaw, Simon Keith. Metal complexes bearing pendant alkynes and metal complexes of N-heterocyclic carbenes.

Degree: PhD, 2004, University of Western Australia

This thesis is comprised of two parts. The first part describes the synthesis of cyclopentadienyltungsten complexes containing a pendant alkyne group (I), and the subsequent… (more)

Subjects/Keywords: Alkynes; Carbenes (Methylene compounds); Metal complexes; Cyclopentadiene; Organometallic chemistry; Synthetic chemistry; Alkyne complexes; N-Heterocyclic carbene complexes; Crystallographic studies; Intramolecular coordination

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APA (6th Edition):

Brayshaw, S. K. (2004). Metal complexes bearing pendant alkynes and metal complexes of N-heterocyclic carbenes. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=7588&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Brayshaw, Simon Keith. “Metal complexes bearing pendant alkynes and metal complexes of N-heterocyclic carbenes.” 2004. Doctoral Dissertation, University of Western Australia. Accessed October 18, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=7588&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Brayshaw, Simon Keith. “Metal complexes bearing pendant alkynes and metal complexes of N-heterocyclic carbenes.” 2004. Web. 18 Oct 2019.

Vancouver:

Brayshaw SK. Metal complexes bearing pendant alkynes and metal complexes of N-heterocyclic carbenes. [Internet] [Doctoral dissertation]. University of Western Australia; 2004. [cited 2019 Oct 18]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=7588&local_base=GEN01-INS01.

Council of Science Editors:

Brayshaw SK. Metal complexes bearing pendant alkynes and metal complexes of N-heterocyclic carbenes. [Doctoral Dissertation]. University of Western Australia; 2004. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=7588&local_base=GEN01-INS01


Case Western Reserve University

103. Heckler, James E. Advances in gold-carbon bond formation: mono-, di-, and triaurated organometallics.

Degree: PhD, Chemistry, 2016, Case Western Reserve University

 Novel auration methods have been developed and used to synthesize new compoundsfeaturing up to three (phosphine)- or (N-heterocyclic carbene)gold(I) fragments bound toaromatic cycles. This has… (more)

Subjects/Keywords: Chemistry; Inorganic Chemistry; Organic Chemistry; gold; transmetalation; cycloaddition; geminal diauration; copper; fluorescence; phosphorescence; heavy atom effect; click chemistry; relativistic effects; triazole; arylboronic acids; alkynyls; azides; DFT; N-heterocyclic carbene; phosphine; aurophilicity

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APA (6th Edition):

Heckler, J. E. (2016). Advances in gold-carbon bond formation: mono-, di-, and triaurated organometallics. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1441363597

Chicago Manual of Style (16th Edition):

Heckler, James E. “Advances in gold-carbon bond formation: mono-, di-, and triaurated organometallics.” 2016. Doctoral Dissertation, Case Western Reserve University. Accessed October 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1441363597.

MLA Handbook (7th Edition):

Heckler, James E. “Advances in gold-carbon bond formation: mono-, di-, and triaurated organometallics.” 2016. Web. 18 Oct 2019.

Vancouver:

Heckler JE. Advances in gold-carbon bond formation: mono-, di-, and triaurated organometallics. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2016. [cited 2019 Oct 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1441363597.

Council of Science Editors:

Heckler JE. Advances in gold-carbon bond formation: mono-, di-, and triaurated organometallics. [Doctoral Dissertation]. Case Western Reserve University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1441363597

104. Tate, Brandon Kyle. Frontiers in the organometallic chemistry of silver: Accessing new structures and reactivity through sterically demanding, electron-rich N-heterocyclic carbene ligands.

Degree: PhD, Chemistry and Biochemistry, 2015, Georgia Tech

 The synthesis and characterization of novel complexes of silver supported by sterically demanding, highly electrophilic N-heterocyclic carbene (NHC) ancillary ligands, is described. Stable hydride, fluoride,… (more)

Subjects/Keywords: Organometallic chemistry; Silver; N-heterocyclic carbene; Renewable energy; Catalysis; Hydrogen activation; Carbon dioxide

…µ mu NHC N-heterocyclic carbene NMR nuclear magnetic resonance ν wavenumber νTEP… …basic N-heterocyclic carbene (NHC) ancillary ligands to stabilize unprecedented… …constant of step n L ligand (see figure caption for definition) L5 1,3-bis(2,6… …bearing symmetrical N-diisopropylphenyl substituents. Silver complexes of these ligands exhibit… …carbene by Arduengo and coworkers,8 is commonly referred to as SIPr or SIDipp (Figure 1.1… 

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APA (6th Edition):

Tate, B. K. (2015). Frontiers in the organometallic chemistry of silver: Accessing new structures and reactivity through sterically demanding, electron-rich N-heterocyclic carbene ligands. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54451

Chicago Manual of Style (16th Edition):

Tate, Brandon Kyle. “Frontiers in the organometallic chemistry of silver: Accessing new structures and reactivity through sterically demanding, electron-rich N-heterocyclic carbene ligands.” 2015. Doctoral Dissertation, Georgia Tech. Accessed October 18, 2019. http://hdl.handle.net/1853/54451.

MLA Handbook (7th Edition):

Tate, Brandon Kyle. “Frontiers in the organometallic chemistry of silver: Accessing new structures and reactivity through sterically demanding, electron-rich N-heterocyclic carbene ligands.” 2015. Web. 18 Oct 2019.

Vancouver:

Tate BK. Frontiers in the organometallic chemistry of silver: Accessing new structures and reactivity through sterically demanding, electron-rich N-heterocyclic carbene ligands. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1853/54451.

Council of Science Editors:

Tate BK. Frontiers in the organometallic chemistry of silver: Accessing new structures and reactivity through sterically demanding, electron-rich N-heterocyclic carbene ligands. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/54451

105. Khalili Najafabadi, Bahareh. Coinage Metal Silylphosphido Complexes Stabilized by N-Heterocyclic Carbene Ligands.

Degree: 2015, University of Western Ontario

N-Heterocyclic carbenes (NHCs) are strong σ-donating ligands and thus, promising candidates for decorating and stabilizing metal-phosphide nanoclusters. While much research has been focused on the… (more)

Subjects/Keywords: N-heterocyclic carbene; silylphosphido; copper; silver phosphide; gold; nanocluster; Inorganic Chemistry

…58 N-Heterocyclic Carbene Stabilized Ag-P Nanoclusters… …millilitre mol mole NHC N-heterocyclic carbene nm nanometre NMR nuclear magnetic resonance… …reactions.7 The first successful isolation of a free N-heterocyclic carbene in 19918 gave the… …phenyl bridged bis-N-heterocyclic carbene ligands (for example see Figure 1-7).47… …NP nanoparticle NSHC N,S-heterocyclic carbenes P-CNHC-P N,N’-diphosphanylimidazol-2… 

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APA (6th Edition):

Khalili Najafabadi, B. (2015). Coinage Metal Silylphosphido Complexes Stabilized by N-Heterocyclic Carbene Ligands. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/3076

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):

Khalili Najafabadi, Bahareh. “Coinage Metal Silylphosphido Complexes Stabilized by N-Heterocyclic Carbene Ligands.” 2015. Thesis, University of Western Ontario. Accessed October 18, 2019. https://ir.lib.uwo.ca/etd/3076.

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

MLA Handbook (7th Edition):

Khalili Najafabadi, Bahareh. “Coinage Metal Silylphosphido Complexes Stabilized by N-Heterocyclic Carbene Ligands.” 2015. Web. 18 Oct 2019.

Vancouver:

Khalili Najafabadi B. Coinage Metal Silylphosphido Complexes Stabilized by N-Heterocyclic Carbene Ligands. [Internet] [Thesis]. University of Western Ontario; 2015. [cited 2019 Oct 18]. Available from: https://ir.lib.uwo.ca/etd/3076.

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

Council of Science Editors:

Khalili Najafabadi B. Coinage Metal Silylphosphido Complexes Stabilized by N-Heterocyclic Carbene Ligands. [Thesis]. University of Western Ontario; 2015. Available from: https://ir.lib.uwo.ca/etd/3076

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

106. YEN SWEE KUAN. SYNTHESIS, STRUCTURE AND CATALYTIC APPLICATION OF NOVEL CARBENE COMPLEXES WITH BENZOTHIAZOLIN-2-YLIDENE LIGANDS.

Degree: 2009, National University of Singapore

Subjects/Keywords: Benzothiazolin-2-ylidene; N; S-Heterocyclic Carbene Complex; Monocarbene; Biscarbene; Mononuclear; Dinuclear; Mix-NSHC-ligand complexes

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APA (6th Edition):

KUAN, Y. S. (2009). SYNTHESIS, STRUCTURE AND CATALYTIC APPLICATION OF NOVEL CARBENE COMPLEXES WITH BENZOTHIAZOLIN-2-YLIDENE LIGANDS. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/17061

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):

KUAN, YEN SWEE. “SYNTHESIS, STRUCTURE AND CATALYTIC APPLICATION OF NOVEL CARBENE COMPLEXES WITH BENZOTHIAZOLIN-2-YLIDENE LIGANDS.” 2009. Thesis, National University of Singapore. Accessed October 18, 2019. http://scholarbank.nus.edu.sg/handle/10635/17061.

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

MLA Handbook (7th Edition):

KUAN, YEN SWEE. “SYNTHESIS, STRUCTURE AND CATALYTIC APPLICATION OF NOVEL CARBENE COMPLEXES WITH BENZOTHIAZOLIN-2-YLIDENE LIGANDS.” 2009. Web. 18 Oct 2019.

Vancouver:

KUAN YS. SYNTHESIS, STRUCTURE AND CATALYTIC APPLICATION OF NOVEL CARBENE COMPLEXES WITH BENZOTHIAZOLIN-2-YLIDENE LIGANDS. [Internet] [Thesis]. National University of Singapore; 2009. [cited 2019 Oct 18]. Available from: http://scholarbank.nus.edu.sg/handle/10635/17061.

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

Council of Science Editors:

KUAN YS. SYNTHESIS, STRUCTURE AND CATALYTIC APPLICATION OF NOVEL CARBENE COMPLEXES WITH BENZOTHIAZOLIN-2-YLIDENE LIGANDS. [Thesis]. National University of Singapore; 2009. Available from: http://scholarbank.nus.edu.sg/handle/10635/17061

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

107. Jang, Hwanjong. Efficient and Selective Synthesis of Multifunctional Organoboron Compounds Promoted by Cu-Based N-Heterocyclic Carbene Complexes.

Degree: PhD, Chemistry, 2016, Boston College

 Chapter 1. We have developed a single-vessel catalytic protocol for double protoboryl additions to terminal alkynes with B2(pin)2 promoted by Cu complex derived from chiral… (more)

Subjects/Keywords: Cu-based complex; multicomponent reaction; N-heterocyclic carbene; organoboron compound; protoboration

…Singaram, B. Acc. Chem. Rec. 1988, 21, 287–293. (c) Miyaura, N.; Suzuki, A. Chem. Rev… …1995, 95, 2457–2483. (d) Miyaura, N. Bull. Chem. Soc. Jpn. 2008, 81, 1535–1553… …reviews on metal-catalyzed diboration, see: (a) Marder, T. B.; Norman, N. C. Top… …Catal. 1998, 5, 63–73. (b) Ishiyama, T.; Miyaura, N. J. Organomet. Chem. 2000, 611… …392–402. (c) Ishiyama, T.; Miyaura, N. Chem. Rec. 2004, 3, 271–280. (d)… 

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APA (6th Edition):

Jang, H. (2016). Efficient and Selective Synthesis of Multifunctional Organoboron Compounds Promoted by Cu-Based N-Heterocyclic Carbene Complexes. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107188

Chicago Manual of Style (16th Edition):

Jang, Hwanjong. “Efficient and Selective Synthesis of Multifunctional Organoboron Compounds Promoted by Cu-Based N-Heterocyclic Carbene Complexes.” 2016. Doctoral Dissertation, Boston College. Accessed October 18, 2019. http://dlib.bc.edu/islandora/object/bc-ir:107188.

MLA Handbook (7th Edition):

Jang, Hwanjong. “Efficient and Selective Synthesis of Multifunctional Organoboron Compounds Promoted by Cu-Based N-Heterocyclic Carbene Complexes.” 2016. Web. 18 Oct 2019.

Vancouver:

Jang H. Efficient and Selective Synthesis of Multifunctional Organoboron Compounds Promoted by Cu-Based N-Heterocyclic Carbene Complexes. [Internet] [Doctoral dissertation]. Boston College; 2016. [cited 2019 Oct 18]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107188.

Council of Science Editors:

Jang H. Efficient and Selective Synthesis of Multifunctional Organoboron Compounds Promoted by Cu-Based N-Heterocyclic Carbene Complexes. [Doctoral Dissertation]. Boston College; 2016. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107188

108. Wu, Hao. Catalytic Enantioselective Formations of C–B, C–C and C–Si Bonds by Organic Molecules or Transition-Metal Complexes.

Degree: PhD, Chemistry, 2015, Boston College

 Catalytic enantioselective reactions are of great importance in synthetic organic chemistry. Thus, development of efficient, selective and easily accessible catalyst for various bond formations is… (more)

Subjects/Keywords: allenyl addition; boryl conjugate addition; copper catalyst; metal free catalyst; N-heterocyclic carbene; silyl conjugate addition

heterocyclic carbene (NHC) first, due to its unique electronic nature: a strong σ donor and… …x28;11) Lawson, Y. G.; Lesley, M. J. G.; Norman, N. C.; Rice, C. R. Marder, T. B. Chem… …6825. (15) (a) Ishiyama, T.; Miyaura, N.; Takahashi, K. Chem. Lett. 2000… …982–983. (b) Ishiyama, T.; Miyaura, N.; Takahashi, K. J. Organomet. Chem. 2001… …Sadighi et al. Ar N N Ar B2(pin)2 n-pentane Cu Ot-Bu Ar = 2,6-diisopropylphenyl… 

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APA (6th Edition):

Wu, H. (2015). Catalytic Enantioselective Formations of C–B, C–C and C–Si Bonds by Organic Molecules or Transition-Metal Complexes. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104759

Chicago Manual of Style (16th Edition):

Wu, Hao. “Catalytic Enantioselective Formations of C–B, C–C and C–Si Bonds by Organic Molecules or Transition-Metal Complexes.” 2015. Doctoral Dissertation, Boston College. Accessed October 18, 2019. http://dlib.bc.edu/islandora/object/bc-ir:104759.

MLA Handbook (7th Edition):

Wu, Hao. “Catalytic Enantioselective Formations of C–B, C–C and C–Si Bonds by Organic Molecules or Transition-Metal Complexes.” 2015. Web. 18 Oct 2019.

Vancouver:

Wu H. Catalytic Enantioselective Formations of C–B, C–C and C–Si Bonds by Organic Molecules or Transition-Metal Complexes. [Internet] [Doctoral dissertation]. Boston College; 2015. [cited 2019 Oct 18]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104759.

Council of Science Editors:

Wu H. Catalytic Enantioselective Formations of C–B, C–C and C–Si Bonds by Organic Molecules or Transition-Metal Complexes. [Doctoral Dissertation]. Boston College; 2015. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104759

109. Bourichon, Damien. Approche théorique de la compréhension de la réactivité de carbènes N-Hétérocycliques vis-à-vis de systèmes (méth)acryliques. Application en polymérisation : Theoretical approach for the comprehension of the N-Heterocyclic carbene’s reactivity to the (meth)acryliques systems. Application for the polymerization.

Degree: Docteur es, Chimie Physique, 2015, Pau

L’objectif principal de cette thèse était de comprendre par une approche conjointe théorie/expérience des réactions de polymérisation de monomères polaires, plus particulièrement de dérivés (méth)acryliques,… (more)

Subjects/Keywords: Carbènes N-Hétérocycliques; (Méth)acrylates; Alcools; Acides de Lewis; Théorie de la Fonctionnelle de la Densité; Dynamique Moléculaire; Profils réactionnels; Couplage expérience-théorie; Catalyse organique; N-Heterocyclic carbene; (Meth)acrylates; Alcohols; Lewis acids; Density Functional Theory (DFT); Molecular Dynamic (MD); Energy profiles; Joint experimental-theoretical approach.ation; Organocatalyzed polymerization

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APA (6th Edition):

Bourichon, D. (2015). Approche théorique de la compréhension de la réactivité de carbènes N-Hétérocycliques vis-à-vis de systèmes (méth)acryliques. Application en polymérisation : Theoretical approach for the comprehension of the N-Heterocyclic carbene’s reactivity to the (meth)acryliques systems. Application for the polymerization. (Doctoral Dissertation). Pau. Retrieved from http://www.theses.fr/2015PAUU3041

Chicago Manual of Style (16th Edition):

Bourichon, Damien. “Approche théorique de la compréhension de la réactivité de carbènes N-Hétérocycliques vis-à-vis de systèmes (méth)acryliques. Application en polymérisation : Theoretical approach for the comprehension of the N-Heterocyclic carbene’s reactivity to the (meth)acryliques systems. Application for the polymerization.” 2015. Doctoral Dissertation, Pau. Accessed October 18, 2019. http://www.theses.fr/2015PAUU3041.

MLA Handbook (7th Edition):

Bourichon, Damien. “Approche théorique de la compréhension de la réactivité de carbènes N-Hétérocycliques vis-à-vis de systèmes (méth)acryliques. Application en polymérisation : Theoretical approach for the comprehension of the N-Heterocyclic carbene’s reactivity to the (meth)acryliques systems. Application for the polymerization.” 2015. Web. 18 Oct 2019.

Vancouver:

Bourichon D. Approche théorique de la compréhension de la réactivité de carbènes N-Hétérocycliques vis-à-vis de systèmes (méth)acryliques. Application en polymérisation : Theoretical approach for the comprehension of the N-Heterocyclic carbene’s reactivity to the (meth)acryliques systems. Application for the polymerization. [Internet] [Doctoral dissertation]. Pau; 2015. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2015PAUU3041.

Council of Science Editors:

Bourichon D. Approche théorique de la compréhension de la réactivité de carbènes N-Hétérocycliques vis-à-vis de systèmes (méth)acryliques. Application en polymérisation : Theoretical approach for the comprehension of the N-Heterocyclic carbene’s reactivity to the (meth)acryliques systems. Application for the polymerization. [Doctoral Dissertation]. Pau; 2015. Available from: http://www.theses.fr/2015PAUU3041

110. McCann, Lucas Charles. Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline.

Degree: PhD, Chemistry, 2016, York University

 Part I: An efficient method for alkyl-alkyl Negishi cross-coupling reaction of unactivated primary alkyl halides with higher-order zincate species (synthesized from dialkylzinc and a non-coordinating… (more)

Subjects/Keywords: Inorganic chemistry; Cross-coupling; Palladium; Zincate; Zinc; Chemistry; Organic chemistry; Methodology; Industrial chemistry; Pd-PEPPSI; PEPPSI; PEPPSI catalyst; Synthesis; Organometallic chemistry; Organometallic; Inorganic; Inorganic chemistry; Scale-up; Process chemistry; Optimization; Negishi; Negishi Cross-coupling; Alkyl-alkyl; Bond formation; NHC; N-heterocyclic carbene; Carbene; Mechanistic determination; Reaction mechanism; Aryl-aryl; Pd-PEPPSI-IPent; Pd-PEPPSI-IHept; Pd-PEPPSI-IPr; Pd-PEPPSI-IPentCl; Pd-PEPPSI-IHeptCl; 2; 6-DI(4-HEPTYL)ANILINE; 6-DI(3-PENTYL)ANILINE; Large-scale

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APA (6th Edition):

McCann, L. C. (2016). Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline. (Doctoral Dissertation). York University. Retrieved from http://hdl.handle.net/10315/32194

Chicago Manual of Style (16th Edition):

McCann, Lucas Charles. “Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline.” 2016. Doctoral Dissertation, York University. Accessed October 18, 2019. http://hdl.handle.net/10315/32194.

MLA Handbook (7th Edition):

McCann, Lucas Charles. “Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline.” 2016. Web. 18 Oct 2019.

Vancouver:

McCann LC. Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline. [Internet] [Doctoral dissertation]. York University; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10315/32194.

Council of Science Editors:

McCann LC. Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline. [Doctoral Dissertation]. York University; 2016. Available from: http://hdl.handle.net/10315/32194

111. Toth, Christopher A. Synthesis of Coupling Substrates for Use in a Highly Enantioselective Conjugated Triene Cyclization Enabled by a Chiral N-Heterocyclic Carbene.

Degree: MS, Chemistry, 2012, Georgia State University

  The ability to generate chiral building blocks is of paramount importance to organic chemists. This problem presents itself most notably at the interface of… (more)

Subjects/Keywords: Asymmetric catalysis; N-heterocyclic carbene; Triene; Enantioselective; Intramolecular stetter reaction; Ethyl (2E) 3-ethyl-4-oxobut-2-enoate

…a N-heterocyclic carbene in situ upon deprotonation (Figure 4). In addition to… …self condensations, N-heterocyclic carbenes have been used effectively to catalyze cross… …by N-heterocyclic carbenes is growing by the day.19 1.2 Discovery of a Novel Asymmetric… …23 viii LIST OF FIGURES Figure 1. Structure of thiamine and its active carbene species… …1 Figure 2. First stable crystalline carbene… 

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APA (6th Edition):

Toth, C. A. (2012). Synthesis of Coupling Substrates for Use in a Highly Enantioselective Conjugated Triene Cyclization Enabled by a Chiral N-Heterocyclic Carbene. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/48

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):

Toth, Christopher A. “Synthesis of Coupling Substrates for Use in a Highly Enantioselective Conjugated Triene Cyclization Enabled by a Chiral N-Heterocyclic Carbene.” 2012. Thesis, Georgia State University. Accessed October 18, 2019. https://scholarworks.gsu.edu/chemistry_theses/48.

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

MLA Handbook (7th Edition):

Toth, Christopher A. “Synthesis of Coupling Substrates for Use in a Highly Enantioselective Conjugated Triene Cyclization Enabled by a Chiral N-Heterocyclic Carbene.” 2012. Web. 18 Oct 2019.

Vancouver:

Toth CA. Synthesis of Coupling Substrates for Use in a Highly Enantioselective Conjugated Triene Cyclization Enabled by a Chiral N-Heterocyclic Carbene. [Internet] [Thesis]. Georgia State University; 2012. [cited 2019 Oct 18]. Available from: https://scholarworks.gsu.edu/chemistry_theses/48.

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

Council of Science Editors:

Toth CA. Synthesis of Coupling Substrates for Use in a Highly Enantioselective Conjugated Triene Cyclization Enabled by a Chiral N-Heterocyclic Carbene. [Thesis]. Georgia State University; 2012. Available from: https://scholarworks.gsu.edu/chemistry_theses/48

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

112. Thiel, Oliver Ralf. Rutheniumkomplexe für die Ringschlußolefinmetathese.

Degree: 2001, Universität Dortmund

Subjects/Keywords: asymmetric synthesis; Asymmetrische Synthese; Balanol; Balanol; catalysis; cross-coupling reactions; Eninmetathese; enyne metathesis; Katalyse; Kreuzkupplungsreaktionen; Lasiodiplodin; Lasiodiplodin; macrocycles; Makrocyclen; natural product synthesis; Naturstoffsynthese; n-heterocyclic carbenes; N-Heterocyclische Carbene; Olefinmetathese; olefin metathesis; Pyrenophorin; Pyrenophorin; ring closing metathesis; Ringschlußmetathese; Ruthenium complexes; Rutheniumkomplexe; Salicylihalamide; Salicylihalamide; Zearaleone; 540

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APA (6th Edition):

Thiel, O. R. (2001). Rutheniumkomplexe für die Ringschlußolefinmetathese. (Thesis). Universität Dortmund. Retrieved from http://hdl.handle.net/2003/2478

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):

Thiel, Oliver Ralf. “Rutheniumkomplexe für die Ringschlußolefinmetathese.” 2001. Thesis, Universität Dortmund. Accessed October 18, 2019. http://hdl.handle.net/2003/2478.

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

MLA Handbook (7th Edition):

Thiel, Oliver Ralf. “Rutheniumkomplexe für die Ringschlußolefinmetathese.” 2001. Web. 18 Oct 2019.

Vancouver:

Thiel OR. Rutheniumkomplexe für die Ringschlußolefinmetathese. [Internet] [Thesis]. Universität Dortmund; 2001. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2003/2478.

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

Council of Science Editors:

Thiel OR. Rutheniumkomplexe für die Ringschlußolefinmetathese. [Thesis]. Universität Dortmund; 2001. Available from: http://hdl.handle.net/2003/2478

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

113. Stelzer, Frank. Totalsynthese von Turrianen - Anwendung und Vergleich von RCM und RCAM.

Degree: 2002, Universität Dortmund

Subjects/Keywords: allyl cation; Allylkation; atom economy; Atomökonomie; cationic reaction pathway; Deuterium labelling; Deuterium-Markierung; DNA-cleaving activity; DNA-spaltende Aktivität; Enine; Enynes; (e/z)-selectivity; (E/Z)-Selektivität; highly substituted biaryl moiety; Hochsubstituierte Biaryleinheit; Kationischer Reaktionsweg; LEWIS acids; LEWIS-Säuren; macrocyclization; Makrocyclisierung; microwave heating; Mikrowellenbestrahlung; natural product synthesis; Naturstoffsynthese; n-heterocyclic carbenes; N-Heterocyclische Carbene; O-C Allyltransfer; O-C allyltransfer; Oxazoline; oxazolines; Platin-katalysierte Cycloisomerisierungen; platinum-catalyzed cycloisomerizations; ring closing alkyne metathesis; ring closing olefin metathesis; Ringschlußalkinmetathese; Ringschluß-olefinmetathese; ruthenium-catalyzed enyne metathesis; Ruthenium-katalysierte Enin-Metathese; turriane; turrianes; vinylcyclopropane; vinylcyclopropanes; 540

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

APA (6th Edition):

Stelzer, F. (2002). Totalsynthese von Turrianen - Anwendung und Vergleich von RCM und RCAM. (Thesis). Universität Dortmund. Retrieved from http://hdl.handle.net/2003/2486

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):

Stelzer, Frank. “Totalsynthese von Turrianen - Anwendung und Vergleich von RCM und RCAM.” 2002. Thesis, Universität Dortmund. Accessed October 18, 2019. http://hdl.handle.net/2003/2486.

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

MLA Handbook (7th Edition):

Stelzer, Frank. “Totalsynthese von Turrianen - Anwendung und Vergleich von RCM und RCAM.” 2002. Web. 18 Oct 2019.

Vancouver:

Stelzer F. Totalsynthese von Turrianen - Anwendung und Vergleich von RCM und RCAM. [Internet] [Thesis]. Universität Dortmund; 2002. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2003/2486.

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

Council of Science Editors:

Stelzer F. Totalsynthese von Turrianen - Anwendung und Vergleich von RCM und RCAM. [Thesis]. Universität Dortmund; 2002. Available from: http://hdl.handle.net/2003/2486

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

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