STRUCTURAL AND SPECTRAL STUDIES OF THE MIXED-LIGAND CATION COMPLEX OF LANTHANUM [Lа(L)2bipy2]BPh4 WITH CARBACYLAMIDOPHOSPHATE (CAPH) TYPE LIGAND AND 2,2'-BIPYRIDINE

M. Struhatska, I. Olyshevets, V. Dyakonenko, V. Ovchynnikov, S. Shishkina, V. Amirkhanov
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Abstract

A new cationic mixed-ligand complex [Lа(L)2bipy2]BPh4 (where L-= bis(N,N'-diethylamide)(N'-trichloroacetyl)-triamidophosphate anion, bipy = 2,2'-bipyridine) has been synthesized and studied by the means of IR, 1H NMR spectroscopy, thermogravimetric and X-ray structural analyses. Low-frequency shifts of the absorption bands of the carbonyl and phosphoryl groups of phosphorylated ligand in the IR spectra of the complex compared with similar absorption bands in the spectrum of "free" CAPh ligand are Δν(C = O) = 117 cm–1 and Δν(P = O) = 137 cm–1. The analysis of integral signal intensity in the investigated NMR spectra of coordination compounds [Lа(L)2bipy2]BPh4 indicates the molar ratio of ligand : bipyridine : tetraphenylborate anion as a 2:2:1, which corresponds to the proposed structure of the complexes. The compound has been obtained in monocrystalline form. The structure of the complex has been determined by X-ray structural analysis, its ionic structure was proved, and the coordination of two CAPh ligands through the oxygen atoms of the carbonyl and phosphoryl groups was confirmed. Based on the structural data, it was determined that the La3+ ion is octocoordinated (surrounded by four oxygen atoms from two chelated phosphoryl ligands and four nitrogen atoms from two 2,2'-bipyridine molecules). The coordination polyhedron of central ion is interpreted as a square antiprism. Complex cations and tetraphenylborate anions are connected both by electrostatic interaction and by weak intermolecular C – H ∙∙∙ π-contacts between phenyl substituents of BPh4- and molecules of 2,2'-bipyridine. It was established by thermogravimetric analysis that the complex [Lа(L)2bipy2]BPh4 obtained is thermally stable up to a temperature of 150 °C. Significant decomposition of the complex begins at a temperature of 150 °C, occurs in one stage and most intensively continues up to 300 °C. The total weight loss is 78 %.
镧[l_ (L)2bipy2]BPh4与碳酰基氨基磷酸(CAPH)型配体和2,2′-联吡啶混合配体阳离子配合物的结构和光谱研究
合成了一种新型阳离子混合配体配合物[l_ (L)2bipy2]BPh4(其中L-=双(N,N′-二乙基酰胺)(N′-三氯乙酰基)-三氨基磷酸阴离子,bipy = 2,2′-联吡啶),并通过红外光谱、1H NMR、热重和x射线结构分析对其进行了研究。在配合物的红外光谱中,磷酸化配体的羰基和磷基的吸收带与“自由”CAPh配体的吸收带相比,低频位移分别为Δν(C = O) = 117 cm-1和Δν(P = O) = 137 cm-1。配位化合物[lfe (L)2bipy2]BPh4的核磁共振谱积分信号强度分析表明配体:联吡啶:四苯基硼酸盐阴离子的摩尔比为2:2:1,与所提出的配合物结构相对应。该化合物以单晶形式得到。通过x射线结构分析确定了配合物的结构,证实了其离子结构,并通过羰基和磷基的氧原子确定了两个CAPh配体的配位。根据结构数据,确定La3+离子是八配位的(由两个螯合磷酰配体的四个氧原子和两个2,2'-联吡啶分子的四个氮原子包围)。中心离子的配位多面体被解释为一个方形反棱镜。配合物阳离子和四苯基硼酸盐阴离子通过静电相互作用和BPh4-的苯基取代基与2,2'-联吡啶分子之间的弱分子间C - H∙∙π-接触连接。热重分析表明,所制得的配合物[lfe (L)2bipy2]BPh4在150℃温度下是热稳定的。该复合物的显著分解始于150°C的温度,发生在一个阶段,最密集地持续到300°C。总体重减轻了78%。
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