Issue 80, 2016

Sigma-spacer regulated thiophenyl triazine conjugates: synthesis and crystal, electronic and luminescent properties

Abstract

A water-accelerated Pd catalyzed Suzuki–Miyaura cross-coupling reaction was developed for the synthesis of thiophenyl triazine conjugates (TTCs). The compounds (2a–2e and 3a–3e) with five σ-spacers were obtained and fully characterized. The X-ray analysis of 2a, 2d, and 3d found that the length of the intermolecular H bond was 3.465(3) Å and the π–π interactions ranged from 3.6538(2)–3.9519(1) Å. Five σ-spacers of TTCs had an effect on their emissions from blue (363 nm) to yellow (530 nm) whilst 2- and 3-thiophenyl chromophores finely tune the emission from 530 to 504 nm. The DFT computation showed the TTCs had low HOMO (−6.8 eV) and LUMO (−2.5 eV) energy and high triplet energy (ET, 2.4 eV). The energy level and gap of TTCs were regularly modulated by the σ-spacer.

Graphical abstract: Sigma-spacer regulated thiophenyl triazine conjugates: synthesis and crystal, electronic and luminescent properties

Supplementary files

Article information

Article type
Paper
Submitted
27 May 2016
Accepted
07 Aug 2016
First published
08 Aug 2016

RSC Adv., 2016,6, 76883-76889

Sigma-spacer regulated thiophenyl triazine conjugates: synthesis and crystal, electronic and luminescent properties

Z. Zhu, E. Shao, S. Xu, H. Sun, G. Zhang, Z. Xie, W. Zhang and Z. Gao, RSC Adv., 2016, 6, 76883 DOI: 10.1039/C6RA13795D

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