Triangular Clusters of Molybdenum Coordinated with Tetrabromocatecholate

Pavel A. Petrov

doi:10.1007/s10876-017-1202-4

Triangular Clusters of Molybdenum Coordinated with Tetrabromocatecholate

Pavel A. Petrov

Кафедра неорганической химии ФЕН

Результат исследования: Научные публикации в периодических изданиях › статья

2 Цитирования (Scopus)

Аннотация

New triangular cluster (Ph₄P)₂[Mo₃S₇(TBC)₃] (2) (TBC—tetrabromocatecholate) was synthesized by the straightforward reaction of (ⁿBu₄N)₂[Mo₃S₇Br₆] (1) with tetrabromocatechol in the presence of Et₃N, followed by the addition of Ph₄PBr. Interaction of 2 with PPh₃ leads to the conversion of the bridging disulphide ligands to the bridging sulphides, and (Ph₄P)₂[Mo₃S₄(TBC)₃(thf)₂]·0.5Et₂O (3·0.5Et₂O) was crystallized out of a THF/Et₂O mixture. The main structural feature of 3 is unsymmetrical environment of the Mo₃ core derived from the coordination of only two THF molecules per three metals.

Язык оригинала	английский
Страницы (с-по)	1815-1823
Число страниц	9
Журнал	Journal of Cluster Science
Том	28
Номер выпуска	4
DOI	https://doi.org/10.1007/s10876-017-1202-4
Состояние	Опубликовано - 1 июл 2017

Доступ к документу

10.1007/s10876-017-1202-4

Link to publication in Scopus

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title = "Triangular Clusters of Molybdenum Coordinated with Tetrabromocatecholate",

abstract = "New triangular cluster (Ph4P)2[Mo3S7(TBC)3] (2) (TBC—tetrabromocatecholate) was synthesized by the straightforward reaction of (nBu4N)2[Mo3S7Br6] (1) with tetrabromocatechol in the presence of Et3N, followed by the addition of Ph4PBr. Interaction of 2 with PPh3 leads to the conversion of the bridging disulphide ligands to the bridging sulphides, and (Ph4P)2[Mo3S4(TBC)3(thf)2]·0.5Et2O (3·0.5Et2O) was crystallized out of a THF/Et2O mixture. The main structural feature of 3 is unsymmetrical environment of the Mo3 core derived from the coordination of only two THF molecules per three metals.",

keywords = "Molybdenum, Redox-active ligands, Sulphur, CATECHOLATE, TRANSITION-METAL-COMPLEXES, COMPONENT MOLECULAR CONDUCTORS, REVERSIBLE BINDING, ALLYL HALIDES, MO3S7 CLUSTERS, LIGANDS, BIS-O-AMIDOPHENOLATE, TRINUCLEAR, BOND",

author = "Petrov, {Pavel A.}",

year = "2017",

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doi = "10.1007/s10876-017-1202-4",

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N2 - New triangular cluster (Ph4P)2[Mo3S7(TBC)3] (2) (TBC—tetrabromocatecholate) was synthesized by the straightforward reaction of (nBu4N)2[Mo3S7Br6] (1) with tetrabromocatechol in the presence of Et3N, followed by the addition of Ph4PBr. Interaction of 2 with PPh3 leads to the conversion of the bridging disulphide ligands to the bridging sulphides, and (Ph4P)2[Mo3S4(TBC)3(thf)2]·0.5Et2O (3·0.5Et2O) was crystallized out of a THF/Et2O mixture. The main structural feature of 3 is unsymmetrical environment of the Mo3 core derived from the coordination of only two THF molecules per three metals.

AB - New triangular cluster (Ph4P)2[Mo3S7(TBC)3] (2) (TBC—tetrabromocatecholate) was synthesized by the straightforward reaction of (nBu4N)2[Mo3S7Br6] (1) with tetrabromocatechol in the presence of Et3N, followed by the addition of Ph4PBr. Interaction of 2 with PPh3 leads to the conversion of the bridging disulphide ligands to the bridging sulphides, and (Ph4P)2[Mo3S4(TBC)3(thf)2]·0.5Et2O (3·0.5Et2O) was crystallized out of a THF/Et2O mixture. The main structural feature of 3 is unsymmetrical environment of the Mo3 core derived from the coordination of only two THF molecules per three metals.

KW - Molybdenum

KW - Redox-active ligands

KW - Sulphur

KW - CATECHOLATE

KW - TRANSITION-METAL-COMPLEXES

KW - COMPONENT MOLECULAR CONDUCTORS

KW - REVERSIBLE BINDING

KW - ALLYL HALIDES

KW - MO3S7 CLUSTERS

KW - LIGANDS

KW - BIS-O-AMIDOPHENOLATE

KW - TRINUCLEAR

KW - BOND

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