COMPLEXATION OF CIS-Pd(NH3)2Cl2 AND Pd(en)Cl2 WITH 1-AMINOPROPYLIDENE­DIPHOSPHONIC ACID

O. Kozachkova, Nataliya Tsaryk, V. Pekhnyo, V. Trachevskij
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Abstract

The complexation of cis-Pd(NH3)2Cl2 and Pd(en)Cl2 (en – ethylenediamine) with 1-aminopropylidene-1,1-diphosphonic acid (APrDP, H4L) in solutions with extracellular concentration of chloride ions (0.15 mol/L) at the rations Pd(II):APrDP=1:1, 1:2 and 2:1 has been stu­di­ed by pH-potentiometry, electron and NMR spectroscopy. It has been found that upon interaction in the system cis-Pd(NH3)2Cl2:AprDP=1:1, complexes of the equimolar composition [PdHL(NH3)Cl]2- (lgβ=38.84(4)), [PdHL(NH3)2]- (lgβ=43.14(2)) and [PdL(NH3)2]2- (lgβ=34.91(2)) are formed depending on pH, in which the APrDP molecule is coordinated in a bidentate fashion to the cent­ral ion by the nitrogen atom of the amine group and oxygen atom of the phosphonic group. In the case of twofold excess of ligand, bisligand complexes [PdH4L2]2- (lgβ=59.64(9)), [PdH3L2]3- (lgβ=57.39(19), [PdH2L2]4- (lgβ=52.37(17), [PdHL2]5- (lgβ=44.71(9)) [PdL2]6- (lgβ=36.57(6)) are formed, in which two APrDP molecules are coordinated in a bidentated fashion. At pH>6, complexes [PdHL2(NH3)]5- (lgβ=48.57(6)) and [PdL2(NH3)2]6- (lgβ=42.76(8)) are formed, in which the coordinated phosphonic groups of APrDP are sequentially replaced upon coordination by NH3. molecules. In the systems Pd(en)Cl2:APrDP=1:1 and 1:2, complexes only of equimolar composition: [Pd(en)(H2L)] (lgβ=28.88(9)), [Pd(en)(HL)]- (lgβ=24.67(8)) and [Pd(en)L]2- (lgβ=16.84(9)) are formed, whose coordination sphere contains the nitrogen atom of the amine group and oxygen atom of the phosphonic group of APrDP and two nitrogen atoms of the amine groups of an ethylenediamine. At the ratio Pd(II):APrDP=2:1, the formation of binuclear complexes {[Pd(NH3)2]2L} (lgβ=63.58(22)) and {[Pd(en)]2L} (lgβ= 25.18(4)), in which two palladium atoms have a different coordination environment. The coordination sphere of one of the palladium contains a nitrogen atom of the amine group and an oxygen atom of the phospho­nic group of APrDP, and two NH3 molecules or two amine groups of ethylenediamine. The other palladium coordinates two oxygen atoms of phoshonic groups of APrDP and two NH3 molecules or two amine groups of ethylenediamine.
顺式钯(NH3)2Cl2和钯(en)Cl2与1-氨基丙烯-二膦酸的络合
用ph电位法、电子能谱法和核磁共振波谱法研究了顺式Pd(NH3)2Cl2和Pd(en)Cl2 (en -乙二胺)与细胞外氯离子浓度为0.15 mol/L、Pd(II):APrDP=1:1、1:2和2:1的1-氨基丙烯-1,1-二膦酸(APrDP, H4L)在细胞外氯离子浓度为Pd(II):APrDP=1:1、1:2和2:1的溶液中的络合反应。在顺式pd (NH3)2Cl2:AprDP=1:1的体系中,随着pH的变化,形成了等摩尔组成的配合物[PdHL(NH3)Cl]2- (lgβ=38.84(4)), [PdHL(NH3)2]- (lgβ=43.14(2))和[PdL(NH3)2]2- (lgβ=34.91(2)),其中AprDP分子通过胺基的氮原子和磷基的氧原子以双齿方式配位到中心离子。在配体双重过量的情况下,形成双配体复合物[PdH4L2]2- (lgβ=59.64(9)), [PdH3L2]3- (lgβ=57.39(19)), [PdH2L2]4- (lgβ=52.37(17)), [PdHL2]5- (lgβ=44.71(9)) [PdL2]6- (lgβ=36.57(6)),其中两个APrDP分子以双齿方式协调。在pH>6时,形成[PdL2(NH3)]5- (lgβ=48.57(6))和[PdL2(NH3)2]6- (lgβ=42.76(8))配合物,其中APrDP的配位膦基依次被NH3取代。分子。在Pd(en)Cl2:APrDP=1:1和1:2的体系中,只形成了等摩尔组成的配合物:[Pd(en)(H2L)] (lgβ=28.88(9)), [Pd(en)(HL)]- (lgβ=24.67(8))和[Pd(en)L]2- (lgβ=16.84(9)),其配位球包含APrDP的胺基氮原子和磷酸基氧原子以及乙二胺的两个胺基氮原子。当Pd(II):APrDP=2:1时,形成了两个钯原子具有不同配位环境的双核配合物{[Pd(NH3)2]2L} (lgβ=63.58(22))和{[Pd(en)]2L} (lgβ= 25.18(4))。其中一个钯的配位球含有APrDP胺基的一个氮原子和磷基的一个氧原子,以及两个NH3分子或两个胺基的乙二胺。另一个钯配位APrDP的两个光子基团氧原子和两个NH3分子或两个胺基乙二胺。
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