Issue 7, 2015

Diverse architectures and luminescence properties of two novel copper(i) coordination polymers assembled from 2,6-bis[3-(pyrid-4-yl)-1,2,4-triazolyl]pyridine ligands

Abstract

Two attractive Cu(I) coordination polymers with unique structures, namely, {[Cu8(bptp)4]·6H2O} (1) and {[Cu5(bptp)2(CN)]·2H2O} (2), have been successfully synthesized based on a V-shaped multidentate N-containing ligand 2,6-bis[3-(pyrid-4-yl)-1,2,4-triazolyl]pyridine (H2bptp). The structural analysis reveals that complex 1 displays a Cu8 cluster-based infinite 1D ladder chain, in which each H2bptp ligand links four or five Cu(I) ions through nitrogen atoms of pyridine/triazole groups. Complex 2 features an unusual (3,4,5)-connected 3D topological network with the Schläfli symbol (42·54·63·7)(42·63·7)(5·6·8)(5·62·7·82), which has not been reported before. The structural and dimensional diversity of the two complexes indicates that H2bptp exhibits strong coordination ability and diverse coordination modes. It is worth mentioning that the Cu⋯Cu distances in 1 and 2 are shorter than the sum of the van der Waals radii of copper(I) (2.80 Å), implying the metal–metal bonding interactions. What is more, the solid-state luminescence bands of 1 and 2 have also been investigated between 298 and 10 K. Interestingly, the low-energy emission bands of 1 and 2 exhibit yellow/orange-red luminescence, and their intensities increase gradually upon cooling.

Graphical abstract: Diverse architectures and luminescence properties of two novel copper(i) coordination polymers assembled from 2,6-bis[3-(pyrid-4-yl)-1,2,4-triazolyl]pyridine ligands

Supplementary files

Article information

Article type
Paper
Submitted
28 Nov 2014
Accepted
02 Jan 2015
First published
07 Jan 2015

CrystEngComm, 2015,17, 1541-1548

Diverse architectures and luminescence properties of two novel copper(I) coordination polymers assembled from 2,6-bis[3-(pyrid-4-yl)-1,2,4-triazolyl]pyridine ligands

J. Pan, C. Liu, F. Jiang, M. Wu, L. Chen, J. Qian, K. Su, X. Wan and M. Hong, CrystEngComm, 2015, 17, 1541 DOI: 10.1039/C4CE02351J

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