H/D solvent isotope effects on the photoracemization reaction of enantiomeric the tris(2,2′-bipyridine)ruthenium(ii) complex and its analogues

被引：4

作者：

Asahara, Masahiro ^{[1
]}

Kurimoto, Haruhiko ^{[1
]}

Nakamizu, Masato ^{[1
]}

Hattori, Shingo ^{[1
]}

Shinozaki, Kazuteru ^{[1
]}

机构：

[1] Yokohama City Univ, Dept Mat Sci, Grad Sch Nanobiosci, Kanazawa Ku, 22-2 Seto, Yokohama, Kanagawa 2360027, Japan

来源：

PHYSICAL CHEMISTRY CHEMICAL PHYSICS | 2020年 / 22卷 / 11期

关键词：

EXCITED-STATE DECAY; CHARGE-TRANSFER; RUTHENIUM(II) COMPLEXES; POLYPYRIDYL COMPLEXES; LIGAND PHOTODISSOCIATION; PHOTOPHYSICAL PROPERTIES; TRIS(2,2-BIPYRIDYL)RUTHENIUM(II) ION; VIBRATIONAL SPECTROSCOPY; ELECTRON DELOCALIZATION; TEMPERATURE-DEPENDENCE;

D O I：

10.1039/c9cp06758b

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

This work assessed solvent isotope effects on the photoracemization rate and emission lifetime for [Ru(bpy)(3)](2+) (bpy = 2,2 '-bipyridine) in water. An analysis of the effects of temperature on photoracemization rate and emission lifetime demonstrated that the transition from one enantiomer to the other is unaffected by the isotopic composition of the solvent. The results also showed that deactivation from the metal-to-ligand charge-transfer ((MLCT)-M-3) excited state to the ground state is responsible for the solvent isotope effect on the photoracemization rate. The photoracemization reaction was found to proceed via a bond-breaking mechanism. In this process, a five-coordinated species produced through breaking of the Ru-N bond in the (3)d-d* state undergoes a structural change to produce an achiral five-coordinated species. An analysis of the effect of temperature on emission lifetime, excluding the activation to the (3)d-d* state that leads to the structural change, showed that the solvent isotopic composition affects deactivation from the 4th MLCT state.

引用

页码：6361 / 6369

页数：9

共 84 条

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