Base-stabilized formally zero-valent mono and diatomic molecular main-group compounds

被引:19
|
作者
Yadav, Ravi [1 ,2 ]
Sinhababu, Soumen [3 ]
Yadav, Ritu [1 ]
Kundu, Subrata [1 ]
机构
[1] Indian Inst Technol Delhi, Dept Chem, New Delhi 110016, India
[2] Heidelberg Univ, Anorg Chem Inst, D-69120 Heidelberg, Germany
[3] Univ Illinois, Dept Chem, 845 W Taylor St, Chicago, IL 60607 USA
关键词
BORON TRIPLE BOND; HETEROCYCLIC-CARBENE; GROUP CHEMISTRY; RADICAL-CATION; DATIVE BONDS; REACTIVITY; NHC; COMPLEXATION; ACTIVATION; ALLENE;
D O I
10.1039/d1dt03569j
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Various compounds are known for transition metals in their formal zero-oxidation state, while similar compounds of main-group elements are recently realized and limited to only a few examples. Lewis-base-stabilized mono and diatomic molecular species (B-2, C, C-2, Si, Si-2, Ge, Ge-2, Sn, P-2, As-2, Sb-2) represent groundbreaking examples of main-group compounds with formally zero-oxidation state. In recent years, the isolation of low-valent main-group compounds has attracted increasing attention of both experimental and theoretical chemists. This is not only due to their fascinating electronic structures and exceptional reactivities, but also their use as valuable precursors for the synthesis of exotic yet important chemical species. This has led to a better understanding of the intricate balance of the donor-acceptor properties of the ligand(s) used to stabilize elements in a formally zero-oxidation state. Owing to the unusual oxidation state of the central element, many compounds containing formally zero-valent elements can efficiently activate otherwise inert small molecules. This review describes the synthesis, characterization, and reactivity of reported mono and diatomic formal zero-oxidation state main-group compounds. This review also emphasizes the comparative description of systems where different ligands are used to stabilize an element in its formal zero-oxidation state.
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页码:2170 / 2202
页数:33
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