Unknown

Dataset Information

0

Light Activated Release of Nitrile Ligands from trans-Ru(L)(PPh3)2(nitrile) Complexes.


ABSTRACT: A series of trans-RuL(PPh3)2(nitrile) and {RuL(PPh3)2}.2-μ-(nitrile)-based complexes [where L = 2,2'-(3,4-diphenyl-pyrrole-2,5-diyl)dipyridine (dpp), di(pyridin-2-yl)isoindoline-1,3-diimine (bpi), or 4-(4-methoxyphenyl)-6-phenyl-2,2'-bipyridine (Pbpy); and nitrile = 1,4-dibenzontirile, 4-ethynylbenzonitrile, or dicyanamide] were synthesized and characterized, and their electrochemical and photochemical behaviors were investigated. Those complexes that contained a significant nitrile contribution to their 3MLLCT show a release of their nitrile ligand (when L = dpp or Pbpy and the nitrile ligand = 4-dibenzontirile, or 4-ethynylbenzonitrile) with dissociation constants up to 8.09 × 10-4 s-1.

SUBMITTER: Davidson RJ 

PROVIDER: S-EPMC11307298 | biostudies-literature | 2024 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

Light Activated Release of Nitrile Ligands from <i>trans</i>-Ru(L)(PPh<sub>3</sub>)<sub>2</sub>(nitrile) Complexes.

Davidson Ross J RJ   Hsu Yu-Ting YT   Yufit Dmitry S DS   Beeby Andrew A  

ACS omega 20240725 31


A series of <i>trans</i>-RuL(PPh<sub>3</sub>)<sub>2</sub>(nitrile) and {RuL(PPh<sub>3</sub>)<sub>2</sub>}.<sub>2</sub>-μ-(nitrile)-based complexes [where L = 2,2'-(3,4-diphenyl-pyrrole-2,5-diyl)dipyridine (dpp), di(pyridin-2-yl)isoindoline-1,3-diimine (bpi), or 4-(4-methoxyphenyl)-6-phenyl-2,2'-bipyridine (Pbpy); and nitrile = 1,4-dibenzontirile, 4-ethynylbenzonitrile, or dicyanamide] were synthesized and characterized, and their electrochemical and photochemical behaviors were investigated. Tho  ...[more]

Similar Datasets

| S-EPMC9554919 | biostudies-literature
| S-EPMC8707700 | biostudies-literature
| S-EPMC8157179 | biostudies-literature
| S-EPMC8155570 | biostudies-literature
| S-EPMC7756557 | biostudies-literature
| S-EPMC9311408 | biostudies-literature
| S-EPMC8447810 | biostudies-literature
| S-EPMC5754034 | biostudies-literature
| S-EPMC4980196 | biostudies-literature
| S-EPMC3882005 | biostudies-literature