Abstract <p>Complexes of copper(I) iodide, bromide, and chloride with N-(diphenylphosphino)-4-phenylpyrimidineamine (L) are synthesized. The [Cu<sub>2</sub>L<sub>2</sub>I<sub>2</sub>] (<b>I</b>), [Cu<sub>2</sub>L<sub>2</sub>I<sub>2</sub>]·2.3MeCN (<b>II</b>), [Cu<sub>2</sub>L<sub>2</sub>Br<sub>2</sub>] ·1.5MeCN·0.5CH<sub>2</sub>Cl<sub>2</sub> (<b>III</b>), and CuLCl (<b>IV</b>) complexes are prepared by reactions of the corresponding copper(I) salts and L in organic solvents in the 1:1 molar ratio. It is shown by XRD that <b>II</b> and <b>III </b>have a binuclear molecular structure; the L molecule is coordinated to copper atoms in a bidentate cyclic mode via P and N1 atoms of the pyrimidine ring; the distorted tetrahedral environment of Cu atoms is supplemented by halide ions; the coordination polyhedron is CuNPI<sub>2</sub> (<b>II)</b> and CuNPBr<sub>2</sub> (<b>III</b>). The structure of <b>II</b> has two crystallographically independent molecules containing a {Cu<sub>2</sub>I<sub>2</sub>} fragment in <i>rhombus</i> and <i>butterfly</i> conformations, respectively. In the molecule of <b>II</b>, all {Cu<sub>2</sub>Br<sub>2</sub>} fragments have a planar rhombic structure. Solid-state photoluminescent properties of L and <b>I</b>, <b>III</b>, <b>IV</b> complexes are studied. The <b>I</b>, <b>III, IV</b> complexes demonstrate single-band red emission with a microsecond lifetime (λ<sub>exc</sub>&#xa0;=&#xa0;400&#xa0;nm) at 635&#xa0;nm, 625&#xa0;nm, and 640&#xa0;nm, respectively. The L compound exhibits solid-state fluorescence with two emission bands at 400&#xa0;nm and 480&#xa0;nm.</p>

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Synthesis, Structure, and Photoluminescent Properties of Copper(I) Complexes with N-(diphenylphosphino)-4-Phenylpyrimidineamine

  • M. D. Taigina,
  • M. I. Rakhmanova,
  • T. S. Sukhikh,
  • K. A. Vinogradova

摘要

Abstract

Complexes of copper(I) iodide, bromide, and chloride with N-(diphenylphosphino)-4-phenylpyrimidineamine (L) are synthesized. The [Cu2L2I2] (I), [Cu2L2I2]·2.3MeCN (II), [Cu2L2Br2] ·1.5MeCN·0.5CH2Cl2 (III), and CuLCl (IV) complexes are prepared by reactions of the corresponding copper(I) salts and L in organic solvents in the 1:1 molar ratio. It is shown by XRD that II and III have a binuclear molecular structure; the L molecule is coordinated to copper atoms in a bidentate cyclic mode via P and N1 atoms of the pyrimidine ring; the distorted tetrahedral environment of Cu atoms is supplemented by halide ions; the coordination polyhedron is CuNPI2 (II) and CuNPBr2 (III). The structure of II has two crystallographically independent molecules containing a {Cu2I2} fragment in rhombus and butterfly conformations, respectively. In the molecule of II, all {Cu2Br2} fragments have a planar rhombic structure. Solid-state photoluminescent properties of L and I, III, IV complexes are studied. The I, III, IV complexes demonstrate single-band red emission with a microsecond lifetime (λexc = 400 nm) at 635 nm, 625 nm, and 640 nm, respectively. The L compound exhibits solid-state fluorescence with two emission bands at 400 nm and 480 nm.