کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1336179 1500223 2016 13 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Spectroscopic and X-ray structural characterization of new organotin carboxylates and their in vitro antifungal activities
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Spectroscopic and X-ray structural characterization of new organotin carboxylates and their in vitro antifungal activities
چکیده انگلیسی

The reactions of SnR2Cl2 (R = Me, Bu or Ph) with sodium 4-phenylbutyrate, NaO2C(CH2)3Ph (NaOPhb), yielded three organotin carboxylates, namely [{(Me2SnOPhb)2O}2] (1), [Bu2Sn(OPhb)2] (2) and [{PhSn(O)OPhb}6] (3). Complexes (1) and (2) have been spectroscopically authenticated by FT-IR, 119Sn Mössbauer, and 1H, 13C{1H} and 119Sn{1H} NMR techniques. In addition, the crystallographic structures of (1)–(3) have been determined by X-ray diffraction measurements. Complex (1) displays two signals in the solution 119Sn NMR spectrum corresponding to the exo (δ −176.3) and endocyclic (δ −188.4) SnMe2 moieties, whereas (2) exhibits only one 119Sn resonance (δ −148.1). The crystallographic characterization of (1) confirms the centrosymmetric tetranuclear stannoxane structure and the existence of the exo and endocyclic SnMe2 moieties in the both distorted trigonal bipyramidal and octahedral environment, respectively. Complex (2) crystallises as a monomer in which the Sn(IV) cation lies at the centre of a distorted octahedron. The bonding scheme in (3) outlines a hexanuclear drum-like structure comprising two six-membered (–Sn–O–)3 stannoxane rings. The supramolecular arrangements of (1)–(3) result from noncovalent interactions, namely Sn⋯O (1) and (2), C–H⋯π (1), and C–H⋯O (1)–(3). Finally, antifungal activities of all organotin derivatives have been screened against Candida albicans (ATCC 18804), Candida tropicalis (ATCC 750), Candida glabrata (ATCC 90030), Candida parapsilosis (ATCC 22019), Candida lusitaniae (CBS 6936), and Candida dubliniensis (clinical isolate 28). Complex (2) exhibited the best biocide activity amongst the three organotin products.

The new complexes: [{(Me2SnOPhb)2O}2] (1), [Bu2Sn(OPhb)2] (2) and [{PhSn(O)OPhb}6] (3), (R = Me, Bu or Ph and −OPhb = −O2C(CH2)3Ph (NaOPhb), have been crystallographically authenticated. Complex (1) displays a stannoxane structure, (2) crystallises as a monomer and (3) outlines a hexanuclear drum-like structure comprising two six-membered (–Sn–O–)3 stannoxane rings.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Polyhedron - Volume 117, 15 October 2016, Pages 35–47
نویسندگان
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