Plumbylidenes
Term · Chemistry · MLC-T-CHM-009046
Divalent lead compounds of formula R2Pb, the lead analogues of carbenes, with lead in the +2 oxidation state and a sextet of valence electrons. Unlike carbenes they are comparatively stable, because lead favours the +2 state over +4 (the inert-pair effect), and species with bulky substituents can be isolated, for example lead(II) bis(trimethylsilyl)amide. Germylidenes and stannylidenes are the lighter analogues.
| Identifier | MLC-T-CHM-009046 |
|---|---|
| Field | Chemistry |
| Subject | Organic and Biomolecular Chemistry |
| Synonyms | plumbylenes |
| References | PAC, 1995, 67, 1307. 'Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995)' on page 1359 (https://doi.org/10.1351/pac199567081307) |
| See also | Carbene analogues |
Record as JSON
{
"id": "MLC-T-CHM-009046",
"term": "Plumbylidenes",
"field": "Chemistry",
"definition": "Divalent lead compounds of formula R2Pb, the lead analogues of carbenes, with lead in the +2 oxidation state and a sextet of valence electrons. Unlike carbenes they are comparatively stable, because lead favours the +2 state over +4 (the inert-pair effect), and species with bulky substituents can be isolated, for example lead(II) bis(trimethylsilyl)amide. Germylidenes and stannylidenes are the lighter analogues.",
"synonyms": [
"plumbylenes"
],
"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 1359 (https://doi.org/10.1351/pac199567081307)"
],
"url": "https://mlchart.com/terminology/chemistry/plumbylidenes/"
}
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