Stannylidenes
Term · Chemistry · MLC-T-CHM-011315
Reactive intermediates with the general formula R2Sn, containing a divalent tin atom bonded to two substituents and possessing two non-bonding electrons. These species are the tin analogues of carbenes and are typically highly reactive and short-lived unless stabilized by bulky substituents or coordination to a metal center. Unstabilized stannylidenes readily undergo insertion reactions or dimerization to form distannenes with a tin-tin double bond.
| Identifier | MLC-T-CHM-011315 |
|---|---|
| Field | Chemistry |
| Subject | Organic and Biomolecular Chemistry |
| Synonyms | stannylenes |
| References | PAC, 1995, 67, 1307. 'Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995)' on page 1366 (https://doi.org/10.1351/pac199567081307) |
| See also | Carbene analogues |
Record as JSON
{
"id": "MLC-T-CHM-011315",
"term": "Stannylidenes",
"field": "Chemistry",
"definition": "Reactive intermediates with the general formula R2Sn, containing a divalent tin atom bonded to two substituents and possessing two non-bonding electrons. These species are the tin analogues of carbenes and are typically highly reactive and short-lived unless stabilized by bulky substituents or coordination to a metal center. Unstabilized stannylidenes readily undergo insertion reactions or dimerization to form distannenes with a tin-tin double bond.",
"synonyms": [
"stannylenes"
],
"subject": "Organic and Biomolecular Chemistry",
"see_also": [
"carbene analogues"
],
"references": [
"PAC, 1995, 67, 1307. 'Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995)' on page 1366 (https://doi.org/10.1351/pac199567081307)"
],
"url": "https://mlchart.com/terminology/chemistry/stannylidenes/"
}
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