Copper(I) and silver(I) complexes of 9,9-dimethyl-4,5-bis(di-tert-butylphosphino) xanthene: photophysical properties and structural rigidity under pressure

被引:29
作者
Keller, Sarah [1 ]
Prescimone, Alessandro [1 ]
Constable, Edwin C. [1 ]
Housecroft, Catherine E. [1 ]
机构
[1] Univ Basel, Dept Chem, BPR 1096,Mattenstr 24a, CH-4058 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
EMITTING ELECTROCHEMICAL-CELLS; SOLID-STATE; CRYSTAL-STRUCTURES; CU(I) COMPLEXES; LIGANDS; FLUORESCENCE; PHOSPHINES; EMITTERS; DESIGN; DIODES;
D O I
10.1039/c7pp00432j
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The heteroleptic complexes [Cu(tBu-xantphos)(bpy)][PF6] and [Ag(tBu-xantphos)(bpy)][PF6], where tBu-xantphos = 9,9-dimethyl-4,5-bis(di-tert-butylphosphino) xanthene and bpy = 2,2'-bipyridine have been synthesized and their photophysical properties investigated. Single crystal X-ray diffraction studies of the compounds under ambient and increased pressure are presented; increase in pressure results in little structural perturbation. For the copper(I) complexes, the effects of changing the (NN)-N-Lambda ligand from bpy to 6-methyl-2,2'-bipyridine (6-Mebpy), 6-bromo-2,2'-bipyridine (6-Brbpy), and 4,4'-di(tert-butyl)-2,2'-bipyridine (4,4'-tBu(2)bpy) were also investigated. Emissions from the copper(I) complexes are weak, both in solution and the solid state and this is attributed to vibrational quenching effects of the tert-butyl sub-stituents of the tBu-xantphos ligands.
引用
收藏
页码:375 / 385
页数:11
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