Tri­fluoro­methane­sulfonate salt of 5,10,15,20-tetra­kis­(1-benzyl­pyridin-1-ium-4-yl)-21H,23H-porphyrin and its CaII complex

IF 0.5 Q4 CRYSTALLOGRAPHY
María K. Salomón-Flores , Josue Valdes-García , Diego Martínez-Otero , Alejandro Dorazco-González , N. Alvarez Failache (Editor)
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引用次数: 0

Abstract

The synthesis and crystallization of a tri­fluoro­methane­sulfonate salt of 5,10,15,20-tetra­kis­(1-benzyl­pyridin-1-ium-4-yl)-21H,23H-porphyrin, C68H54N8 4+·4CF3O3S·4H2O, 1·OTf, are reported. The asymmetric unit contains half a porphyrin mol­ecule, two tri­fluoro­methane­sulfonate anions and two water mol­ecules of crystallization. The macrocycle of tetra­pyrrole moieties is planar and unexpectedly it has coordinated CaII ions in occupational disorder. This CaII ion has only 10% occupancy (C72H61.80Ca0.10F12N8O16S4).

The synthesis, crystallization and characterization of a tri­fluoro­methane­sulfonate salt of 5,10,15,20-tetra­kis­(1-benzyl­pyridin-1-ium-4-yl)-21H,23H-por­phy­rin, C68H54N8 4+·4CF3SO3 ·4H2O, 1·OTf, are reported in this work. The reaction between 5,10,15,20-tetra­kis­(pyridin-4-yl)-21H,23H-porphyrin and benzyl bromide in the presence of 0.1 equiv. of Ca(OH)2 in CH3CN under reflux with an N2 atmosphere and subsequent treatment with silver tri­fluoro­methane­sulfonate (AgOTf) salt produced a red–brown solution. This reaction mixture was filtered and the solvent was allowed to evaporate at room temperature for 3 d to give 1·OTf. Crystal structure determination by single-crystal X-ray diffraction (SCXD) revealed that 1·OTf crystallizes in the space group P21/c. The asymmetric unit contains half a porphyrin mol­ecule, two tri­fluoro­methane­sulfonate anions and two water mol­ecules of crystallization. The macrocycle of tetra­pyrrole moieties is planar and unexpectedly it has coordinated CaII ions in occupational disorder. This CaII ion has only 10% occupancy (C72H61.80Ca0.10F12N8O16S4). The pyridinium rings bonded to methyl­ene groups from porphyrin are located in two different arrangements in almost orthogonal positions between the plane formed by the porphyrin and the pyridinium rings. The crystal structure features cation⋯π inter­actions between the CaII atom and the π-system of the phenyl ring of neighboring mol­ecules. Both tri­fluoro­methane­sulfonate anions are found at the periphery of 1, forming hydrogen bonds with water mol­ecules.

5,10,15,20-四(1-苄基吡啶-1-鎓-4-基)-21H,23H-卟啉的三氟甲磺酸盐及其 CaII 复合物
本文报道了 5,10,15,20-四(1-苄基吡啶-1-鎓-4-基)-21H,23H-卟啉的三氟甲磺酸盐 C68H54N8 4+-4CF3SO3 --4H2O, 1-OTf 的合成、结晶和表征。5,10,15,20-四(吡啶-4-基)-21H,23H-卟啉和溴化苄在 0.1 等量 Ca(OH)2 的存在下于 CH3CN 中反应,在 N2 气氛下回流,随后用三氟甲磺酸银 (AgOTf) 盐处理,生成红棕色溶液。过滤反应混合物,让溶剂在室温下蒸发 3 d,得到 1-OTF。通过单晶 X 射线衍射(SCXD)进行的晶体结构测定显示,1-OTF 晶体的空间群为 P21/c。不对称单元包含半个卟啉分子、两个三氟甲磺酸阴离子和两个结晶水分子。四吡咯分子的大循环是平面的,出乎意料的是,它在占位紊乱中具有配位的 CaII 离子。这种 CaII 离子的占有率只有 10%(C72H61.80Ca0.10F12N8O16S4)。与卟啉亚甲基键合的吡啶鎓环以两种不同的排列方式位于卟啉和吡啶鎓环形成的平面之间几乎正交的位置。晶体结构的特点是 CaII 原子与邻近分子苯环的 π 系统之间存在阳离子......π 相互作用。两个三氟甲磺酸阴离子都位于 1 的外围,与水分子形成氢键。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
351
审稿时长
3 weeks
期刊介绍: Acta Crystallographica Section E: Crystallographic Communications is the IUCr''s open-access structural communications journal. It provides a fast, simple and easily accessible publication mechanism for crystal structure determinations of inorganic, metal-organic and organic compounds. The electronic submission, validation, refereeing and publication facilities of the journal ensure rapid and high-quality publication of fully validated structures. The primary article category is Research Communications; these are peer-reviewed articles describing one or more structure determinations with appropriate discussion of the science.
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