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- W2892096277 endingPage "43" @default.
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- W2892096277 abstract "The isolation of a rare and highly unstable silicon(II) dihalide using N-heterocyclic carbene (NHC) proved to be a landmark achievement in the field of silicon chemistry. The first stable NHC stabilized halosilylene was isolated and structurally characterized in 2009. Subsequently the study of NHC stabilized halosilylenes over the past nine years has opened-up a new dimension in the field of organosilicon chemistry. NHC stabilized halosilylene compounds have been extensively used as starting materials for the synthesis of rare organosilicon compounds like small ring systems with high ring-strain energy containing silicon (silaoxirane), C4-silyl substituted NHC, Si–Si multiple bond, molecule with rare Si–M bond (M = main group or transition metals), dichlorosilamines (SiN), silaisontriles, trisilaallenes (silicon analogue of allene) etc. These studies clearly demonstrated the potential applications of NHC stabilized halosilylenes in various fields of organosilicon chemistry. The present review summarizes the progress and scope of NHC-halosilylene chemistry. In particular, an overview of synthetic strategies, spectral properties, key structural features and available bonding analysis are discussed." @default.
- W2892096277 created "2018-09-27" @default.
- W2892096277 creator A5031101992 @default.
- W2892096277 creator A5045449975 @default.
- W2892096277 creator A5060691139 @default.
- W2892096277 creator A5080913126 @default.
- W2892096277 date "2018-12-01" @default.
- W2892096277 modified "2023-09-23" @default.
- W2892096277 title "N-heterocyclic carbene supported halosilylenes: New frontiers in an emerging field" @default.
- W2892096277 cites W118837172 @default.
- W2892096277 cites W1598737486 @default.
- W2892096277 cites W1821032334 @default.
- W2892096277 cites W1907767300 @default.
- W2892096277 cites W1965017955 @default.
- W2892096277 cites W1967266229 @default.
- W2892096277 cites W1971080513 @default.
- W2892096277 cites W1972206365 @default.
- W2892096277 cites W1973105379 @default.
- W2892096277 cites W1973446797 @default.
- W2892096277 cites W1977431288 @default.
- W2892096277 cites W1981892156 @default.
- W2892096277 cites W1982637863 @default.
- W2892096277 cites W1985542788 @default.
- W2892096277 cites W1988099159 @default.
- W2892096277 cites W1988883484 @default.
- W2892096277 cites W1989637340 @default.
- W2892096277 cites W1993885846 @default.
- W2892096277 cites W1996939043 @default.
- W2892096277 cites W2003143283 @default.
- W2892096277 cites W2004249279 @default.
- W2892096277 cites W2005227604 @default.
- W2892096277 cites W2014104145 @default.
- W2892096277 cites W2014447405 @default.
- W2892096277 cites W2014467142 @default.
- W2892096277 cites W2026697041 @default.
- W2892096277 cites W2030441366 @default.
- W2892096277 cites W2030841140 @default.
- W2892096277 cites W2031363452 @default.
- W2892096277 cites W2032908030 @default.
- W2892096277 cites W2036687381 @default.
- W2892096277 cites W2036803366 @default.
- W2892096277 cites W2042125006 @default.
- W2892096277 cites W2046286719 @default.
- W2892096277 cites W2050505061 @default.
- W2892096277 cites W2055053833 @default.
- W2892096277 cites W2060968988 @default.
- W2892096277 cites W2066032829 @default.
- W2892096277 cites W2067728662 @default.
- W2892096277 cites W2067769697 @default.
- W2892096277 cites W2068653676 @default.
- W2892096277 cites W2072105154 @default.
- W2892096277 cites W2073963192 @default.
- W2892096277 cites W2074305691 @default.
- W2892096277 cites W2078231424 @default.
- W2892096277 cites W2080383853 @default.
- W2892096277 cites W2086296254 @default.
- W2892096277 cites W2086507774 @default.
- W2892096277 cites W2089395684 @default.
- W2892096277 cites W2092307593 @default.
- W2892096277 cites W2093530361 @default.
- W2892096277 cites W2107619799 @default.
- W2892096277 cites W2110298104 @default.
- W2892096277 cites W2110502363 @default.
- W2892096277 cites W2113273359 @default.
- W2892096277 cites W2115135661 @default.
- W2892096277 cites W2121826018 @default.
- W2892096277 cites W2122375910 @default.
- W2892096277 cites W2125534637 @default.
- W2892096277 cites W2126795015 @default.
- W2892096277 cites W2130824840 @default.
- W2892096277 cites W2134649862 @default.
- W2892096277 cites W2135089750 @default.
- W2892096277 cites W2136630731 @default.
- W2892096277 cites W2137485994 @default.
- W2892096277 cites W2138081664 @default.
- W2892096277 cites W2146984773 @default.
- W2892096277 cites W2150844649 @default.
- W2892096277 cites W2156279531 @default.
- W2892096277 cites W2161151883 @default.
- W2892096277 cites W2165931506 @default.
- W2892096277 cites W2171208686 @default.
- W2892096277 cites W2192085021 @default.
- W2892096277 cites W2312205328 @default.
- W2892096277 cites W2314684690 @default.
- W2892096277 cites W2315621616 @default.
- W2892096277 cites W2319605794 @default.
- W2892096277 cites W2328351571 @default.
- W2892096277 cites W2329167113 @default.
- W2892096277 cites W2329493704 @default.
- W2892096277 cites W2329524472 @default.
- W2892096277 cites W2329586383 @default.
- W2892096277 cites W2330241726 @default.
- W2892096277 cites W2343766415 @default.
- W2892096277 cites W2510438590 @default.
- W2892096277 cites W2527742357 @default.
- W2892096277 cites W2591141861 @default.
- W2892096277 cites W2605049812 @default.
- W2892096277 cites W2616914310 @default.