المؤلفون: Dominika Lastovickova, Christopher Bielawski

المصدر: Catalysts; Volume 6; Issue 9; Pages: 141

مصطلحات موضوعية: hydroboration, carbenes, organocatalysis, Lewis adducts, diamidocarbene

وصف الملف: application/pdf

Relation: https://dx.doi.org/10.3390/catal6090141

الاتاحة: https://doi.org/10.3390/catal6090141

المؤلفون: César, Vincent, Lugan, Noël, Lavigne, Guy

المساهمون: Laboratoire de chimie de coordination (LCC), Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS)

المصدر: ISSN: 1434-1948.

مصطلحات موضوعية: Heterocyclic carbenes, Diamidocarbene, Organometallic chemistry, [CHIM.COOR]Chemical Sciences/Coordination chemistry

Relation: hal-03710153; https://hal.science/hal-03710153; https://hal.science/hal-03710153/document; https://hal.science/hal-03710153/file/C%C3%A9sar,%20Reprogramming%20of%20a%20malonic%20N-heterocyclic%20carbene,%202010.pdf

الاتاحة: https://hal.science/hal-03710153
https://hal.science/hal-03710153/document
https://hal.science/hal-03710153/file/C%C3%A9sar,%20Reprogramming%20of%20a%20malonic%20N-heterocyclic%20carbene,%202010.pdf
https://doi.org/10.1002/ejic.200901113

المؤلفون: Song, Hayoung, Kim, Hyunho, Lee, Eunsung

المساهمون: Song, Hayoung, Kim, Hyunho, Lee, Eunsung

مصطلحات موضوعية: CYCLIC (ALKYL)(AMINO)CARBENES CAACS, ALKYL AMINO CARBENES, STABLE CARBENES, LIGANDS, COMPLEXES, BACKBONE, N,N&apos, DIAMIDOCARBENE, ELECTROPHILICITY, DIAMINOCARBENE, ACTIVATION, carbenes, ligand design, main-group elements, synthetic methods, transition metals

Relation: Angewandte Chemie - International Edition; Chemistry, Multidisciplinary; Chemistry; https://oasis.postech.ac.kr/handle/2014.oak/99271; 32206; Angewandte Chemie - International Edition, v.57, no.28, pp.8603 - 8607; 000437668700042; 2-s2.0-85049571369

الاتاحة: https://oasis.postech.ac.kr/handle/2014.oak/99271
https://doi.org/10.1002/anie.201804249

المؤلفون: Moerdyk, Jonathan Philip

Thesis Advisors: Bielawski, Christopher W.

مصطلحات موضوعية: Carbene, Diamidocarbene

وصف الملف: application/pdf

الاتاحة: http://hdl.handle.net/2152/30451

المؤلفون: Zhao, Fei, Wang, Yang, Xu, Ling, Zhang, Wen-Xiong, Xi, Zhenfeng

المساهمون: Zhang, WX (reprint author), Peking Univ, Coll Chem, Minist Educ, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China., Peking Univ, Coll Chem, Minist Educ, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China., Peking Univ, Coll Chem, Minist Educ, Key Lab Bioorgan Chem & Mol Engn, Beijing 100871, Peoples R China., Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China.

المصدر: SCI

مصطلحات موضوعية: Carbodiimide, Diamidocarbene, 2,2-Dichloroimidazolidine-4,5-dione, Copper DAC complex, 2-Selenoxoimidazolidine-4,5-dione, 2,2-Difluoroimidazolidine-4,5-dione, N-HETEROCYCLIC CARBENE, C-H, GEM-DIHALOCYCLOPROPANES, SELECTIVE SYNTHESIS, CATALYZED REACTIONS, ORGANIC-SYNTHESIS, BUILDING-BLOCKS, CARBODIIMIDES, AMINO, POLYMERIZATION

Relation: TETRAHEDRON LETTERS.2014,55,(33),4597-4600.; 771055; http://hdl.handle.net/20.500.11897/210846; WOS:000340018600020

الاتاحة: https://hdl.handle.net/20.500.11897/210846
https://doi.org/10.1016/j.tetlet.2014.06.095

المؤلفون: Charlotte Riley, Nguyen Le Phuoc, Mikko Linnolahti, Alexander S. Romanov

مصطلحات موضوعية: Biophysics, Biochemistry, Molecular Biology, Biotechnology, Hematology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, neutral trigold cluster, fast radiative rates, bright phosphorescent emitters, 4 × 10, )­ cl revealed, 5 , pseudohalide gold complexes, pseudohalide complexes, tert <, n <, linear gold, gold atom, tddft calculations, strong base, solid state, photophysical properties, nucleophilic attack, neighboring molecules, intrinsic π, high yields, diamidocarbene ligand

Relation: https://figshare.com/articles/journal_contribution/Linear_Gold_I_Halide_Complexes_with_a_Diamidocarbene_Ligand_Synthesis_Reactivity_and_Phosphorescence/24595805

الاتاحة: https://doi.org/10.1021/acs.organomet.3c00360.s001
https://figshare.com/articles/journal_contribution/Linear_Gold_I_Halide_Complexes_with_a_Diamidocarbene_Ligand_Synthesis_Reactivity_and_Phosphorescence/24595805