Bis[5-(anthracen-9-ylmeth­yl)-1,5,9-tri­aza­cyclododecan-1-ium] tetra­chlorido­zincate

IUCrData Pub Date : 2025-05-01 DOI:10.1107/S2414314625003566
Yoshimi Ichimaru , Koichi Kato , Wanchun Jin , Masaaki Kurihara , Hiromasa Kurosaki
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引用次数: 0

Abstract

The structure of the title salt comprising two monoprotonated polyamine ligands and one tetra­chloro­zincate(II) anion was analyzed and compared with those of structurally related compounds bearing different macrocyclic frameworks and pendant arms. The protonated nitro­gen atoms engaged in intra­molecular hydrogen bonding with other nitro­gen atoms within the macrocyclic ring.
A crystalline salt comprising two monoprotonated polyamine ligands and one tetra­chloro­zincate(II) anion was prepared, (C24H32N3)2[ZnCl4], and its crystal structure was analyzed and compared with those of structurally related compounds bearing different macrocyclic frameworks and pendant arms. The protonated nitro­gen atoms engaged in intra­molecular hydrogen bonding with other nitro­gen atoms within the macrocyclic ring. In the crystal, the pendant anthracene groups participated in inter­molecular π–π and C—H⋯π inter­actions, contributing to crystal cohesion.
  1. Download: Download high-res image (265KB)
  2. Download: Download full-size image
国际清算银行[5 - (anthracen-9-ylmeth-yl) 1、5、9-tri-aza-cyclododecan-1-ium] tetra-chlorido-zincate。
制备了一种由两个单质子化多胺配体和一个四氯锌酸盐(II)阴离子组成的结晶盐(C24H32N3)2[ZnCl4],并对其晶体结构进行了分析,并与具有不同大环框架和垂臂的结构相关化合物进行了比较。质子化的氮原子在分子内与大环内的其他氮原子形成氢键。在晶体中,悬垂的蒽基团参与分子间π-π和C-H⋯π的相互作用,有助于晶体的内聚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.30
自引率
0.00%
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