SiP-heterocycles derived from a bulky phosphanylsilylene
Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArC&z.tbd;CR (Ar = Ph, 4-iPr-C 6 H 4 , 3-F-C 6 H 4 ; R = H, Ph) at 80 °C under microwave irradiation to afford fluorescence-active SiP-heterocycles 3a-d , which may undergo unique isomerizations starting from silirene intermediates. Moreover,...
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Published in | Chemical communications (Cambridge, England) Vol. 59; no. 68; pp. 1275 - 1278 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
CAMBRIDGE
Royal Soc Chemistry
22.08.2023
Royal Society of Chemistry |
Subjects | |
Online Access | Get full text |
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Summary: | Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArC&z.tbd;CR (Ar = Ph, 4-iPr-C
6
H
4
, 3-F-C
6
H
4
; R = H, Ph) at 80 °C under microwave irradiation to afford fluorescence-active SiP-heterocycles
3a-d
, which may undergo unique isomerizations starting from silirene intermediates. Moreover, the treatment of
1
with AdC&z.tbd;P furnished a heavy congener of cyclopentadiene (
4
), whose formation involves cleavage of the Si(
ii
)-P bond that is rarely observed in silylene chemistry.
A new bis(1-adamantyl)phosphanylsilylene was synthesized and reacted with alkynes and a phosphaalkyne to furnish different Si-P heterocyclic complexes. |
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Bibliography: | Electronic supplementary information (ESI) available. CCDC 2204071 For ESI and crystallographic data in CIF or other electronic format see DOI 2223430 2204070 and 2204068 2223427 2223428 https://doi.org/10.1039/d3cc02512h , 2277645 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1359-7345 1364-548X 1364-548X |
DOI: | 10.1039/d3cc02512h |