Journal Article
Research Support, Non-U.S. Gov't
Add like
Add dislike
Add to saved papers

A stable heavier group 14 analogue of vinylidene.

Nature Chemistry 2016 November
Vinylidene (H2 C=C) is a member of the family of compounds of composition CH (and isomeric with ethyne, HC≡CH), but it has been observed only transiently-with a lifetime in the region of 0.1 ns. Indeed, no simple (non-base-stabilized) compounds of the type R2 E=E have been characterized structurally for any of the group 14 elements. Here we show that by employing the bulky and strongly electron-donating boryl ligand (HCDippN)2 B (Dipp, 2,6-i Pr2 C6 H3 ), a simple monomeric digermavinylidene compound, (boryl)2 GeGe, can be synthesized and is stable at room temperature. Both its formation via the two-electron chemical oxidation of the symmetrical Ge0 compound K2 [(boryl)GeGe(boryl)] and its subsequent reaction chemistry (for example, with H2 ), are consistent with a high substituent lability and the accessibility of both 1,1- and 1,2-substitution patterns. Structural and computational studies of [(HCDippN)2 B]2 GeGe reveal a weak Ge-Ge double bond-the π component of which contributes to the highest occupied molecular orbital (HOMO)-with a Ge-centred lone pair as the HOMO-1.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app