Structural diversity in multinuclear tantalum polyhydrides formed via reductive hydrogenolysis of metal–carbon bonds

2019 ◽  
Vol 55 (88) ◽  
pp. 13263-13266 ◽  
Author(s):  
Jade I. Fostvedt ◽  
Trevor D. Lohrey ◽  
Robert G. Bergman ◽  
John Arnold

Put the methyl to the metal: hydrogenolysis of metal–carbon bonds offers controlled access to low-valent early metal complexes.

2021 ◽  
Author(s):  
Rong Zhang ◽  
Yanchao Wang ◽  
Yanxia Zhao ◽  
Carl Redshaw ◽  
Igor L. Fedushkin ◽  
...  

The use of dad (and bian) ligands in the stabilization of main-group complexes, in particular metal–metal-bonded compounds, as well as the small molecule reactivity of these (low-valent) metal complexes, is summarized.


1985 ◽  
Vol 40 (9) ◽  
pp. 1181-1187 ◽  
Author(s):  
Yvonne Nagel ◽  
Wolfgang Beck

The reaction of bis(2,3,4,6-tetra-0-acetyl-β-D-glucopyranosyl)disulfide with (Ph3P)2Pt(C2H4) gives cis-di(2,3,4,6-tetra-0-acetyl-l-mercapto-β-D-glucopyranosid)bis(triphenylphosphane)platinum (II). A dithiocarbimato complex (Ph3P)2Pt(S2CNR) has been isolated from cis-(Ph3P)2PtCl2, CS2 and 1-0-Methyl-2-amino-2-deoxy-4,6-benzyliden-α,β-D-glucopyranoside. Metal complexes with metal-carbon bonds have been prepared by oxidative addition of monosaccharide halides to (Ph3P)2Pt(C2H4) or to cobalt(I) cobaloxime, respectively. From the reaction of (Ph3P)2Pt(C2H4) with 2,3,4,6 -Tetra-O-acetyl-α-D-glucopyranosyl-bromide the anomers trans-(α- and β-glucopyranosyl) Pt(PPh3)2Br have been obtained. This indicates a radical reaction.


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