Suppr超能文献

银(I)-铜(I)炔基-二膦配合物的合成、光物理和理论研究。

Synthesis, photophysical and theoretical studies of luminescent silver(I)-copper(I) alkynyl-diphosphine complexes.

机构信息

University of Joensuu, Joensuu, 80101, Finland.

出版信息

Dalton Trans. 2010 Mar 7;39(9):2395-403. doi: 10.1039/b920856a. Epub 2010 Jan 14.

Abstract

The novel heterometallic aggregates [Ag(8)Cu(2)(C(2)C(6)H(4)X)(6)(PPh(2)C(6)H(4)PPh(2))(6)]PF(6) (X = H, 1; OMe, 2; NMe(2), 3) were prepared by the self-assembly reactions starting from simple precursors. These compounds consist of the central Ag(6)Cu(2)(C(2)C(6)H(4)X)(6) clusters capped by two tripodal fragments Ag(diphosphine)(3). The solid state structures of complexes 1 and 3 have been determined by X-ray crystallographic studies, and NMR spectroscopy confirmed that the compounds remain intact in solution. In solution such as CH(3)CN, complexes 1-3 show a weak to moderate room-temperature phosphorescence in the blue region with a maximum quantum yield of 0.038 (2), while strong phosphorescence was recorded in the solid film of with a quantum yield of 0.26. Photophysical experiments revealed a relatively small effect of luminescence quenching by O(2) for 1, but more prominent quenching for 2 and 3 in solution. Computational approaches are in good agreement with the experimental data, supporting the proposed structural motif, and provide an additional insight into the electronic properties of these compounds to rationalize the different behavior of 1 compared to 2 and 3.

摘要

新型杂金属聚合体 [Ag(8)Cu(2)(C(2)C(6)H(4)X)(6)(PPh(2)C(6)H(4)PPh(2))(6)]PF(6) (X = H, 1; OMe, 2; NMe(2), 3) 是通过自组装反应从简单的前体制备而成的。这些化合物由中央 Ag(6)Cu(2)(C(2)C(6)H(4)X)(6) 簇组成,由两个三脚片段 Ag(diphosphine)(3) 封端。配合物 1 和 3 的固态结构已通过 X 射线晶体学研究确定,NMR 光谱证实这些化合物在溶液中保持完整。在 CH(3)CN 等溶液中,配合物 1-3 在蓝色区域显示出弱至中等室温磷光,最大量子产率为 0.038(2),而在固体薄膜中记录到强磷光,量子产率为 0.26。光物理实验表明,1 对氧气的发光猝灭影响相对较小,但 2 和 3 在溶液中的猝灭更为明显。计算方法与实验数据吻合良好,支持所提出的结构模式,并为这些化合物的电子性质提供了额外的见解,以解释 1 与 2 和 3 相比的不同行为。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验