These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Changes in ligating abilities of the singlet and triplet states of normal, abnormal and remote N-heterocyclic carbenes depending on their aromaticities. Sevinçek R; Karabıyık H; Karabıyık H J Mol Model; 2013 Dec; 19(12):5327-41. PubMed ID: 24305725 [TBL] [Abstract][Full Text] [Related]
4. Effect of substituents at the heteroatom on the structure and ligating properties of heterocyclic carbene, silylene, germylene and abnormal carbene: a theoretical study. Guha AK; Sarmah S; Phukan AK Dalton Trans; 2010 Aug; 39(31):7374-83. PubMed ID: 20607170 [TBL] [Abstract][Full Text] [Related]
5. Electronic and Ligand Properties of Skeletally Substituted Cyclic (Alkyl)(Amino)Carbenes (CAACs) and Their Reactivity towards Small Molecule Activation: A Theoretical Study. Bharadwaz P; Chetia P; Phukan AK Chemistry; 2017 Jul; 23(41):9926-9936. PubMed ID: 28504835 [TBL] [Abstract][Full Text] [Related]
6. A novel ylide-stabilized carbene; formation and electron donating ability of an amino(sulfur-ylide)carbene. Kobayashi J; Nakafuji SY; Yatabe A; Kawashima T Chem Commun (Camb); 2008 Dec; (46):6233-5. PubMed ID: 19082130 [TBL] [Abstract][Full Text] [Related]
7. Electronic and ligating properties of carbocyclic carbenes: A theoretical investigation. Bhagat S; Arfeen M; Das G; Patel N; Bharatam PV J Comput Chem; 2018 Dec; ():. PubMed ID: 30549074 [TBL] [Abstract][Full Text] [Related]
8. Experimental and theoretical investigations on the high-electron donor character of pyrido-annelated N-heterocyclic carbenes. Nonnenmacher M; Buck DM; Kunz D Beilstein J Org Chem; 2016; 12():1884-1896. PubMed ID: 27829895 [TBL] [Abstract][Full Text] [Related]
12. Electronic and ligand properties of annelated normal and abnormal (mesoionic) N-heterocyclic carbenes: a theoretical study. Phukan AK; Guha AK; Sarmah S; Dewhurst RD J Org Chem; 2013 Nov; 78(21):11032-9. PubMed ID: 24102531 [TBL] [Abstract][Full Text] [Related]
13. Direct estimate of the internal π-donation to the carbene centre within N-heterocyclic carbenes and related molecules. Andrada DM; Holzmann N; Hamadi T; Frenking G Beilstein J Org Chem; 2015; 11():2727-36. PubMed ID: 26877795 [TBL] [Abstract][Full Text] [Related]
14. Azavinylidenephosphoranes: a class of cyclic push-pull carbenes. Lavigne F; El Kazzi A; Escudié Y; Maerten E; Kato T; Saffon-Merceron N; Branchadell V; Cossío FP; Baceiredo A Chemistry; 2014 Sep; 20(39):12528-36. PubMed ID: 25123091 [TBL] [Abstract][Full Text] [Related]
15. QTAIM analysis of ligand properties and mechanisms of tuning of 6-membered ring N-heterocyclic carbenes in transition metal complexes through ring-substituent variation. Johnson LE; DuPré DB J Phys Chem A; 2009 Jul; 113(30):8647-53. PubMed ID: 19548646 [TBL] [Abstract][Full Text] [Related]
16. Reactivity of cyclic (alkyl)(amino)carbenes (CAACs) and bis(amino)cyclopropenylidenes (BACs) with heteroallenes: comparisons with their N-heterocyclic carbene (NHCs) counterparts. Kuchenbeiser G; Soleilhavoup M; Donnadieu B; Bertrand G Chem Asian J; 2009 Nov; 4(11):1745-50. PubMed ID: 19780080 [TBL] [Abstract][Full Text] [Related]
17. Imidazo[1,5-a]pyridin-3-ylidenes as π-accepting carbene ligands: substituent effects on properties of N-heterocyclic carbenes. Koto Y; Shibahara F; Murai T Org Biomol Chem; 2017 Feb; 15(8):1810-1820. PubMed ID: 28155955 [TBL] [Abstract][Full Text] [Related]
18. N-Heterocyclic carbene or phosphorus ylide: which one forms a stronger bond with group 11 metals? A theoretical study. Bayat M; Sedghi A; Ebrahimkhani L; Sabounchei SJ Dalton Trans; 2016 Dec; 46(1):207-220. PubMed ID: 27924996 [TBL] [Abstract][Full Text] [Related]
19. How to make the σ0π2 singlet the ground state of carbenes. Chen B; Rogachev AY; Hrovat DA; Hoffmann R; Borden WT J Am Chem Soc; 2013 Sep; 135(37):13954-64. PubMed ID: 24007553 [TBL] [Abstract][Full Text] [Related]
20. Modulating the Bonding Properties of N-Heterocyclic Carbenes (NHCs): A Systematic Charge-Displacement Analysis. Gaggioli CA; Bistoni G; Ciancaleoni G; Tarantelli F; Belpassi L; Belanzoni P Chemistry; 2017 Jun; 23(31):7558-7569. PubMed ID: 28370714 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]