Deep-red phosphorescent organic-inorganic hybrid Mn(II) complexes based on 2-(diphenylphosphoryl)-N,N-diethylacetamide ligand

被引:24
作者
Artem'ev, Alexander, V [1 ]
Berezin, Alexey S. [1 ]
Brel, Valery K. [2 ]
Morgalyuk, Vasily P. [2 ]
Samsonenko, Denis G. [1 ,3 ]
机构
[1] Russian Acad Sci, Nikolaev Inst Inorgan Chem, Siberian Branch, 3 Akad Lavrentiev Ave, Novosibirsk 630090, Russia
[2] Russian Acad Sci, Nesmeyanov Inst Elementorgan Cpds, Vavilova Str 28, Moscow 119991, Russia
[3] Novosibirsk State Univ, Natl Res Univ, Dept Nat Sci, 2 Pirogova Str, Novosibirsk 630090, Russia
基金
俄罗斯基础研究基金会;
关键词
Manganese; Organic-inorganic hybrid complexes; Phosphorescence; Deep-red emission; Mn(II) halides; LIGHT EMISSION; TRIBOLUMINESCENCE; LUMINESCENCE; PHOTOLUMINESCENCE;
D O I
10.1016/j.poly.2018.04.012
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two unprecedented organic-inorganic hybrid complexes, [Mn(L)(3)]MnCl4 (1) and [Mn(L)(3)]MnBr4 (2), have been synthesized in 88-92% yields via reaction of Mn(II) halides with Ph-2 P(0)CH2 C(O)NEt2 (L) in a 3:2 M ratio. X-ray diffraction analysis of 2 reveals that the metal ion of the [Mn(L)(3)](2+ )cation has an octahedral geometry, while the [MnBr4] (2-) anion contains tetrahedrally coordinated Mn(II). At ambient temperature, the solid complexes 1 and 2 exhibit bright deep-red phosphorescence (lambda(em)(max) = 660 and 670 nm) with the lifetimes of 3-3.7 ms and photoluminescence quantum yields of 6% and 27%, respectively. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:184 / 188
页数:5
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