OUT-OF-PLANE COORDINATED ZIRCONIUM(IV) AND HAFNIUM(IV) PHTHALOCYANINATES

V. Chernii, I. Tretyakova, Larysa Tomachynska, Y. Gerasymchuk, S. Chernii, V. Pekhnyo
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Abstract

The article is devoted to methods of synthesis, the structure, and spectral characteristics of zirconium and hafnium phthalocyaninates with out-of-plane coordinated ligands. The gene­ral scheme for the synthesis of out-of-plane coordinated Zr and Hf phthalocyanines includes obtaining initial dichloride or dihydroxo complexes, which then undergo substitution reactions with -dicarbonyl compounds, hydroxybenzoic, sulfo- and aliphatic carboxylic acids, etc. In the case of polyphenols, which are bidentate ligands, one ligand is coordinated to the central atom of the macrocycle. If -dicarbonyl compounds or carboxylic acids are introduced into the reaction, two ligands are coordinated. The reactivity of the out-of-plane coordinated ligands of Zr and Hf phthalocyanines was also investigated. In all obtained out-of-plane coordinated Zr and Hf phthalocyanines, the ligands are located in the cis position relative to the plane of the phthalocyanine macrocycle. X-ray diffraction, NMR, and UV-Vis spectroscopy have proved this arrangement of ligands. According to the X-ray diffraction data of Zr and Hf dibenzoylmethanato phthalocyanines, the metal atom is out of the plane of the phthalocyanine macrocycle, which itself is not planar. The central atoms are located almost in the middle between the N4 planes of the phthalocyanine macrocycle and the O4 of the extraplanar li­gands. The UV-Vis spectra of out-of-plane coordinated Zr and Hf phthalocyanines in organic solvents have a typical appearance for most metal phthalocyanines, characterized by a B-band of absorption in the region of 335–350 nm, a Q-band at 680-690 nm, and its satellite in the region of 615–620 nm. If the extraplanar ligand is a chromophore (e.g., curcumin or condensed derivatives of dehydroacetic acid), there are additional absorption bands in  UV-Vis spectra located between the B- and Q-bands. The influence of the nature of the central metal atoms, ligands and solvents on the fluorescent properties of the out-of-plane coordinated Zr and Hf phthalocyanines was also discussed.
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面外配位酞菁酸锆(iv)和铪(iv)
本文介绍了具有面外配位体的酞菁酸锆和酞菁酸铪的合成方法、结构和光谱特性。合成面外配位Zr和Hf酞菁的一般方案包括获得初始二氯或二羟基配合物,然后与-二羰基化合物、羟基苯甲酸、磺酰羧酸和脂肪族羧酸等进行取代反应。多酚是双齿配体,其中一个配体与大环的中心原子配位。如果在反应中引入-二羰基化合物或羧酸,则两个配体是配位的。研究了Zr和Hf酞菁的面外配体的反应性。在所有得到的平面外配位的Zr和Hf酞菁中,配体相对于酞菁大环的平面处于顺式位置。x射线衍射、核磁共振和紫外可见光谱证明了配体的这种排列。根据Zr和Hf二苯甲酰甲烷酞菁的x射线衍射数据,金属原子在酞菁大环的平面外,而酞菁大环本身不是平面的。中心原子几乎位于酞菁大环的N4平面和平面外锂基团的O4平面之间的中间。在有机溶剂中,平面外配位的Zr和Hf酞菁的紫外可见光谱具有大多数金属酞菁的典型特征,在335 ~ 350 nm处有b波段吸收,在680 ~ 690 nm处有q波段吸收,在615 ~ 620 nm处有卫星波段吸收。如果面外配体是发色团(例如姜黄素或脱氢乙酸的缩合衍生物),则在UV-Vis光谱中位于B-和q -波段之间有额外的吸收带。讨论了中心金属原子、配体和溶剂的性质对平面外配位Zr和Hf酞菁荧光性能的影响。
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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