Crystal structures of two (5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane)iron(III) complexes

被引：4

作者：

Clendening, Reese A. ^{[1
]}

Zeller, Matthias ^{[1
]}

Ren, Tong ^{[1
]}

机构：

[1] Purdue Univ, Dept Chem, 560 Oval Dr, W Lafayette, IN 47907 USA

来源：

ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY | 2019年 / 75卷

基金：

美国国家科学基金会;

关键词：

iron(III); tetraazacyclotetradecane; crystal structure; cis configuration; trans configuration; CO-III(CYCLAM); TET;

D O I：

10.1107/S2053229619013925

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Reported in this contribution are the synthesis and crystal structures of two new Fe-III complexes of 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane (HMC), namely, dichlorido(5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane)iron(III) chloride, [FeCl2(C16H36N4)]Cl or cis-[FeCl2(rac-HMC)]Cl (1), and dichlorido(5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane)iron(III) tetrachloridoferrate, [FeCl2(C16H36N4)][FeCl4] or trans-[FeCl2(meso-HMC)][FeCl4] (2). Single-crystal X-ray diffraction studies revealed that both 1 and 2 adopt a pseudo-octahedral geometry, where the macrocycles adopt folded and planar geometries, respectively. The chloride ligands in 1 are cis to each other, while those in 2 have a trans configuration. The relevant bond angles in 1 deviate substantially from an ideal octahedral coordination geometry, with the angles between the cis substituents varying from 81.55 (5) to 107.56 (4)degrees, and those between the trans-ligating atoms varying from 157.76 (8) to 170.88 (3)degrees. In contrast, 2 adopts a less strained configuration, in which the N-Fe-N angles vary from 84.61 (8) to 95.39 (8)degrees and the N-Fe-Cl angles vary from 86.02 (5) to 93.98 (5)degrees.

引用

页码：1509 / +

页数：18

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