An unprecedented, reversible coordination mode rearrangement: η3(B-H) vs. η1(Sn) stanna-closo-dodecaborate coordination

Torben Gädt; Lars Wesemann

doi:10.1039/b514203m

An unprecedented, reversible coordination mode rearrangement: η³(B-H) vs. η¹(Sn) stanna-closo-dodecaborate coordination

Torben Gädt
, Lars Wesemann

University of Tübingen

Research output: Contribution to journal › Article › peer-review

11 Scopus citations

Abstract

The synthesis of the ruthenium stanna-closo-dodecaborate complex by an unprecedented, reversible η³(B-H) to η¹(Sn) rearrangement of (Bu₃MeN)₂[Ru(dppb)SnB₁₁H ₁₁)₂] is described. The product is characterized by multinuclear NMR spectroscopy and single crystal X-ray diffraction. The η¹(Sn) to η³(B-H) reaction can be compared with S-P rearrangements in the coordination chemistry of heterocycles. It is concluded that stanna-closo-dodecaborate is a versatile ligand in coordination chemistry and the first example of a reversible η³ (B-H) to η¹(E) (E:heteroatom) rearrangement is established.

Original language	English
Pages (from-to)	328-329
Number of pages	2
Journal	Dalton Transactions
Issue number	2
DOIs	https://doi.org/10.1039/b514203m
State	Published - 2006
Externally published	Yes

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title = "An unprecedented, reversible coordination mode rearrangement: η3(B-H) vs. η1(Sn) stanna-closo-dodecaborate coordination",

abstract = "The synthesis of the ruthenium stanna-closo-dodecaborate complex by an unprecedented, reversible η3(B-H) to η1(Sn) rearrangement of (Bu3MeN)2[Ru(dppb)SnB11H 11)2] is described. The product is characterized by multinuclear NMR spectroscopy and single crystal X-ray diffraction. The η1(Sn) to η3(B-H) reaction can be compared with S-P rearrangements in the coordination chemistry of heterocycles. It is concluded that stanna-closo-dodecaborate is a versatile ligand in coordination chemistry and the first example of a reversible η3 (B-H) to η1(E) (E:heteroatom) rearrangement is established.",

author = "Torben G{\"a}dt and Lars Wesemann",

year = "2006",

doi = "10.1039/b514203m",

language = "English",

pages = "328--329",

journal = "Dalton Transactions",

issn = "1477-9226",

publisher = "Royal Society of Chemistry",

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T1 - An unprecedented, reversible coordination mode rearrangement

T2 - η3(B-H) vs. η1(Sn) stanna-closo-dodecaborate coordination

AU - Gädt, Torben

AU - Wesemann, Lars

PY - 2006

Y1 - 2006

N2 - The synthesis of the ruthenium stanna-closo-dodecaborate complex by an unprecedented, reversible η3(B-H) to η1(Sn) rearrangement of (Bu3MeN)2[Ru(dppb)SnB11H 11)2] is described. The product is characterized by multinuclear NMR spectroscopy and single crystal X-ray diffraction. The η1(Sn) to η3(B-H) reaction can be compared with S-P rearrangements in the coordination chemistry of heterocycles. It is concluded that stanna-closo-dodecaborate is a versatile ligand in coordination chemistry and the first example of a reversible η3 (B-H) to η1(E) (E:heteroatom) rearrangement is established.

AB - The synthesis of the ruthenium stanna-closo-dodecaborate complex by an unprecedented, reversible η3(B-H) to η1(Sn) rearrangement of (Bu3MeN)2[Ru(dppb)SnB11H 11)2] is described. The product is characterized by multinuclear NMR spectroscopy and single crystal X-ray diffraction. The η1(Sn) to η3(B-H) reaction can be compared with S-P rearrangements in the coordination chemistry of heterocycles. It is concluded that stanna-closo-dodecaborate is a versatile ligand in coordination chemistry and the first example of a reversible η3 (B-H) to η1(E) (E:heteroatom) rearrangement is established.

UR - https://www.scopus.com/pages/publications/33645523463

U2 - 10.1039/b514203m

DO - 10.1039/b514203m

M3 - Article

AN - SCOPUS:33645523463

SN - 1477-9226

SP - 328

EP - 329

JO - Dalton Transactions

JF - Dalton Transactions

IS - 2

ER -

An unprecedented, reversible coordination mode rearrangement: η³(B-H) vs. η¹(Sn) stanna-closo-dodecaborate coordination

Abstract

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