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 |
|---|---|
| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
CAMBRIDGE
Royal Soc Chemistry
22.08.2023
Royal Society of Chemistry |
| Subjects | |
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| Abstract | 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. |
|---|---|
| AbstractList | Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArCCR (Ar = Ph, 4-iPr-C6H4, 3-F-C6H4; 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 AdCP furnished a heavy congener of cyclopentadiene (4), whose formation involves cleavage of the Si(II)-P bond that is rarely observed in silylene chemistry.Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArCCR (Ar = Ph, 4-iPr-C6H4, 3-F-C6H4; 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 AdCP furnished a heavy congener of cyclopentadiene (4), whose formation involves cleavage of the Si(II)-P bond that is rarely observed in silylene chemistry. Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArC≡CR (Ar = Ph, 4-iPr-C6H4, 3-F-C6H4; 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≡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. Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArC CR (Ar = Ph, 4-iPr-C6H4, 3-F-C6H4; R = H, Ph) at 80 degrees 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 Ad RP furnished a heavy congener of cyclopentadiene (4), whose formation involves cleavage of the Si(II)-P bond that is rarely observed in silylene chemistry. Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArCCR (Ar = Ph, 4-iPr-C H , 3-F-C H ; 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 AdCP furnished a heavy congener of cyclopentadiene (4), whose formation involves cleavage of the Si(II)-P bond that is rarely observed in silylene chemistry. 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. Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArCCR (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 AdCP furnished a heavy congener of cyclopentadiene (4), whose formation involves cleavage of the Si( ii )–P bond that is rarely observed in silylene chemistry. |
| Author | Wang, Chenfeng Su, Ming-Der Zuo, Darui Zhang, Zheng-Feng Li, Yan Zhang, Haoqi Zhou, Jiahao Fang, Zijie Li, Xiaodi |
| AuthorAffiliation | College of Material, Chemistry and Chemical Engineering Ministry of Education Hangzhou Normal University National Chiayi University Kaohsiung Medical University Key Laboratory of Organosilicon Chemistry and Material Technology Key Laboratory of Silicone Materials Technology of Zhejiang Province Department of Applied Chemistry Department of Medicinal and Applied Chemistry |
| AuthorAffiliation_xml | – sequence: 0 name: National Chiayi University – sequence: 0 name: Kaohsiung Medical University – sequence: 0 name: Key Laboratory of Organosilicon Chemistry and Material Technology – sequence: 0 name: Ministry of Education – sequence: 0 name: Department of Medicinal and Applied Chemistry – sequence: 0 name: Hangzhou Normal University – sequence: 0 name: Key Laboratory of Silicone Materials Technology of Zhejiang Province – sequence: 0 name: Department of Applied Chemistry – sequence: 0 name: College of Material, Chemistry and Chemical Engineering |
| Author_xml | – sequence: 1 givenname: Chenfeng surname: Wang fullname: Wang, Chenfeng – sequence: 2 givenname: Ming-Der surname: Su fullname: Su, Ming-Der – sequence: 3 givenname: Zijie surname: Fang fullname: Fang, Zijie – sequence: 4 givenname: Jiahao surname: Zhou fullname: Zhou, Jiahao – sequence: 5 givenname: Haoqi surname: Zhang fullname: Zhang, Haoqi – sequence: 6 givenname: Xiaodi surname: Li fullname: Li, Xiaodi – sequence: 7 givenname: Darui surname: Zuo fullname: Zuo, Darui – sequence: 8 givenname: Zheng-Feng surname: Zhang fullname: Zhang, Zheng-Feng – sequence: 9 givenname: Yan surname: Li fullname: Li, Yan |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37539464$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1039_D4DT01367K crossref_primary_10_1002_zaac_202400116 crossref_primary_10_1021_acs_inorgchem_4c02384 crossref_primary_10_1039_D4CS00101J |
| Cites_doi | 10.1016/j.ccr.2013.10.005 10.1002/anie.200600647 10.1002/hc.20705 10.1039/c39810000191 10.1021/ja00385a019 10.1021/acs.inorgchem.2c01762 10.1002/anie.201811088 10.1021/jacs.2c11204 10.1038/s44160-023-00279-6 10.1021/cr100216y 10.1021/ja1054912 10.1021/ja9091374 10.1039/B618515K 10.1039/C4CC05905K 10.1021/acs.inorgchem.2c03140 10.1039/b609250k 10.1002/anie.201812592 10.1039/C9DT03185E 10.1021/ja205369h 10.1039/D0CS00815J 10.1021/acs.organomet.0c00368 10.1002/anie.202115570 10.1002/anie.201104146 10.1039/c0cc01753a 10.1002/anie.201201581 10.1002/chem.201001141 10.1002/anie.201005866 10.1039/B411438H 10.1002/chem.202201963 10.1016/j.orgel.2003.08.006 10.1515/znb-2018-0121 10.1021/ar9900562 10.1016/S0010-8545(03)00098-5 10.1002/1521-3773(20000703)39:13<2307::AID-ANIE2307>3.0.CO;2-D 10.1002/anie.202009638 10.1021/acs.inorgchem.1c00188 10.1002/tcr.200900011 10.1021/om3003762 10.1021/ja074019e 10.1002/anie.201502531 10.1021/cr00099a007 10.1002/anie.201803888 10.1039/C7TC02511D 10.1002/anie.200400655 10.1021/ar300196u 10.1021/ja200462y 10.1039/c9dt03185e 10.1002/anie.202114598 10.1039/b411438h 10.1039/d0cs00815j 10.1039/c4cc05905k 10.1039/b618515k 10.1039/c7tc02511d |
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| Keywords | SILYLENE ACTIVATION BOND CLEAVAGE DERIVATIVES CATION HIGH-EFFICIENCY ACCESS |
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| References | Shan (D3CC02512H/cit1b/1) 2020; 49 Rodriguez (D3CC02512H/cit16c/1) 2012; 51 Hahn (D3CC02512H/cit10b/1) 2000; 39 Ghadwal (D3CC02512H/cit3c/1) 2013; 46 Hayashi (D3CC02512H/cit22a/1) 2009; 9 Rödl (D3CC02512H/cit22b/1) 2018; 73 Regitz (D3CC02512H/cit8a/1) 1990; 90 Wang (D3CC02512H/cit18b/1) 2006; 16 D3CC02512H/cit19/1 Liu (D3CC02512H/cit10c/1) 2019; 48 Liu (D3CC02512H/cit14/1) 2023; 62 Zhu (D3CC02512H/cit2f/1) 2021; 60 Goicoechea (D3CC02512H/cit8c/1) 2018; 57 Chirila (D3CC02512H/cit8b/1) 2014; 270–271 Sen (D3CC02512H/cit12/1) 2011; 50 So (D3CC02512H/cit2b/1) 2007; 129 Du (D3CC02512H/cit20b/1) 2022; 61 Brook (D3CC02512H/cit21a/1) 1981 Herrington (D3CC02512H/cit22c/1) 2014; 50 Chen (D3CC02512H/cit5b/1) 2020; 39 Sen (D3CC02512H/cit11/1) 2011; 50 Gau (D3CC02512H/cit16a/1) 2010; 132 Yeong (D3CC02512H/cit5a/1) 2010; 16 Ishida (D3CC02512H/cit16b/1) 2011; 22 Sen (D3CC02512H/cit2c/1) 2010; 132 Asay (D3CC02512H/cit1a/1) 2011; 111 Zhang (D3CC02512H/cit2g/1) 2022; 144 Hissler (D3CC02512H/cit3b/1) 2003; 244 Liu (D3CC02512H/cit10d/1) 2019; 58 Xiong (D3CC02512H/cit7/1) 2023; 2 Inoue (D3CC02512H/cit15/1) 2011; 133 Nakajima (D3CC02512H/cit10a/1) 2015; 54 Franz (D3CC02512H/cit3a/1) 2000; 33 Brook (D3CC02512H/cit21b/1) 1982; 104 So (D3CC02512H/cit2a/1) 2006; 45 Sen (D3CC02512H/cit13/1) 2011; 133 Palilis (D3CC02512H/cit18a/1) 2003; 4 Sun (D3CC02512H/cit20a/1) 2022; 28 Jones (D3CC02512H/cit9/1) 2007 Liu (D3CC02512H/cit6/1) 2022; 61 Sarkar (D3CC02512H/cit2e/1) 2020; 59 Azhakar (D3CC02512H/cit23/1) 2012; 31 Sen (D3CC02512H/cit4/1) 2010; 46 Kappe (D3CC02512H/cit17a/1) 2004; 43 Cai (D3CC02512H/cit18c/1) 2017; 5 de la Hoz (D3CC02512H/cit17a/2) 2005; 34 Zhou (D3CC02512H/cit2d/1) 2019; 58 Liu, LL (WOS:000488472000004) 2019; 48 Zhu, KK (WOS:000653539100037) 2021; 60 Chen, X (WOS:000753976500003) 2022; 61 Inoue, S (WOS:000289455200020) 2011; 133 Hissler, M (WOS:000186381800001) 2003; 244 Kappe, CO (WOS:000225575600006) 2004; 43 Sen, SS (WOS:000288036300021) 2011; 50 So, CW (WOS:000249887700037) 2007; 129 Zhou, YP (WOS:000462680700006) 2019; 58 Ishida, S (WOS:000291910600023) 2011; 22 Liu, CH (WOS:000920930200001) 2022; 61 Gau, D (WOS:000282013700028) 2010; 132 Sarkar, SK (WOS:000579476500001) 2020; 59 Liu, R (WOS:000914746700001) 2023; 62 Palilis, LC (WOS:000186977000008) 2003; 4 Azhakar, R (WOS:000305588000026) 2012; 31 Jones, C (WOS:000246312000011) 2007 Sen, SS (WOS:000298332700014) 2011; 50 BROOK, AG (WOS:A1982PL96900019) 1982; 104 Rodriguez, R (WOS:000306314300016) 2012; 51 Shan, CK (WOS:000571350600010) 2020; 49 So, CW (WOS:000238501500010) 2006; 45 Hahn, FE (WOS:000088181900020) 2000; 39 Sen, SS (WOS:000280658300007) 2010; 46 Cai, YJ (WOS:000406848400001) 2017; 5 Herrington, TJ (WOS:000342990400040) 2014; 50 Hayashi, M (WOS:000271136800003) 2009; 9 Goicoechea, JM (WOS:000454575500006) 2018; 57 REGITZ, M (WOS:A1990CP98500008) 1990; 90 Sen, SS (WOS:000275084700041) 2010; 132 Chirila, A (WOS:000336013800005) 2014; 270 BROOK, AG (WOS:A1981LD16900032) 1981 Liu, LL (WOS:000455818400041) 2019; 58 Franz, AK (WOS:000165603800009) 2000; 33 Nakajima, K (WOS:000356390900024) 2015; 54 Zhang, Y (WOS:000898842500001) 2022; 144 Asay, M (WOS:000287620600004) 2011; 111 Chen, YL (WOS:000599997800025) 2020; 39 Wang, EG (WOS:000241516700008) 2006; 16 Xiong, Y (WOS:001124816600001) 2023; 2 Sun, XF (WOS:000835372600001) 2022; 28 de la Hoz, A (WOS:000226522500006) 2005; 34 Ghadwal, RS (WOS:000315478700024) 2013; 46 Yeong, HX (WOS:000284063900026) 2010; 16 Sen, SS (WOS:000293768400077) 2011; 133 Rodl, C (WOS:000448777600018) 2018; 73 |
| References_xml | – volume: 270–271 start-page: 57 year: 2014 ident: D3CC02512H/cit8b/1 publication-title: Coord. Chem. Rev. doi: 10.1016/j.ccr.2013.10.005 – volume: 45 start-page: 3948 year: 2006 ident: D3CC02512H/cit2a/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.200600647 – volume: 22 start-page: 432 year: 2011 ident: D3CC02512H/cit16b/1 publication-title: Heteroat. Chem. doi: 10.1002/hc.20705 – ident: D3CC02512H/cit19/1 – start-page: 191 year: 1981 ident: D3CC02512H/cit21a/1 publication-title: J. Chem. Soc., Chem. Commun. doi: 10.1039/c39810000191 – volume: 104 start-page: 5667 year: 1982 ident: D3CC02512H/cit21b/1 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00385a019 – volume: 61 start-page: 15864 year: 2022 ident: D3CC02512H/cit6/1 publication-title: Inorg. Chem. doi: 10.1021/acs.inorgchem.2c01762 – volume: 58 start-page: 3715 year: 2019 ident: D3CC02512H/cit2d/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201811088 – volume: 144 start-page: 22446 year: 2022 ident: D3CC02512H/cit2g/1 publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.2c11204 – volume: 2 start-page: 678 year: 2023 ident: D3CC02512H/cit7/1 publication-title: Nat. Synth. doi: 10.1038/s44160-023-00279-6 – volume: 111 start-page: 354 year: 2011 ident: D3CC02512H/cit1a/1 publication-title: Chem. Rev. doi: 10.1021/cr100216y – volume: 132 start-page: 12841 year: 2010 ident: D3CC02512H/cit16a/1 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja1054912 – volume: 132 start-page: 1123 year: 2010 ident: D3CC02512H/cit2c/1 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja9091374 – start-page: 1929 year: 2007 ident: D3CC02512H/cit9/1 publication-title: Dalton Trans. doi: 10.1039/B618515K – volume: 50 start-page: 12753 year: 2014 ident: D3CC02512H/cit22c/1 publication-title: Chem. Commun. doi: 10.1039/C4CC05905K – volume: 62 start-page: 1095 year: 2023 ident: D3CC02512H/cit14/1 publication-title: Inorg. Chem. doi: 10.1021/acs.inorgchem.2c03140 – volume: 16 start-page: 4133 year: 2006 ident: D3CC02512H/cit18b/1 publication-title: J. Mater. Chem. doi: 10.1039/b609250k – volume: 58 start-page: 273 year: 2019 ident: D3CC02512H/cit10d/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201812592 – volume: 48 start-page: 14242 year: 2019 ident: D3CC02512H/cit10c/1 publication-title: Dalton Trans. doi: 10.1039/C9DT03185E – volume: 133 start-page: 12311 year: 2011 ident: D3CC02512H/cit13/1 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja205369h – volume: 49 start-page: 6733 year: 2020 ident: D3CC02512H/cit1b/1 publication-title: Chem. Soc. Rev. doi: 10.1039/D0CS00815J – volume: 39 start-page: 4282 year: 2020 ident: D3CC02512H/cit5b/1 publication-title: Organometallics doi: 10.1021/acs.organomet.0c00368 – volume: 61 start-page: e202115570 year: 2022 ident: D3CC02512H/cit20b/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.202115570 – volume: 50 start-page: 12510 year: 2011 ident: D3CC02512H/cit12/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201104146 – volume: 46 start-page: 5873 year: 2010 ident: D3CC02512H/cit4/1 publication-title: Chem. Commun. doi: 10.1039/c0cc01753a – volume: 51 start-page: 7158 year: 2012 ident: D3CC02512H/cit16c/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201201581 – volume: 16 start-page: 12956 year: 2010 ident: D3CC02512H/cit5a/1 publication-title: Chem. – Eur. J. doi: 10.1002/chem.201001141 – volume: 50 start-page: 2322 year: 2011 ident: D3CC02512H/cit11/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201005866 – volume: 34 start-page: 164 year: 2005 ident: D3CC02512H/cit17a/2 publication-title: Chem. Soc. Rev. doi: 10.1039/B411438H – volume: 28 start-page: e202201963 year: 2022 ident: D3CC02512H/cit20a/1 publication-title: Chem. – Eur. J. doi: 10.1002/chem.202201963 – volume: 4 start-page: 113 year: 2003 ident: D3CC02512H/cit18a/1 publication-title: Org. Electron. doi: 10.1016/j.orgel.2003.08.006 – volume: 73 start-page: 895 year: 2018 ident: D3CC02512H/cit22b/1 publication-title: Z. Naturforsch. B doi: 10.1515/znb-2018-0121 – volume: 33 start-page: 813 year: 2000 ident: D3CC02512H/cit3a/1 publication-title: Acc. Chem. Res. doi: 10.1021/ar9900562 – volume: 244 start-page: 1 year: 2003 ident: D3CC02512H/cit3b/1 publication-title: Coord. Chem. Rev. doi: 10.1016/S0010-8545(03)00098-5 – volume: 39 start-page: 2307 year: 2000 ident: D3CC02512H/cit10b/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/1521-3773(20000703)39:13<2307::AID-ANIE2307>3.0.CO;2-D – volume: 59 start-page: 23015 year: 2020 ident: D3CC02512H/cit2e/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.202009638 – volume: 60 start-page: 7143 year: 2021 ident: D3CC02512H/cit2f/1 publication-title: Inorg. Chem. doi: 10.1021/acs.inorgchem.1c00188 – volume: 9 start-page: 236 year: 2009 ident: D3CC02512H/cit22a/1 publication-title: Chem. Record doi: 10.1002/tcr.200900011 – volume: 31 start-page: 4588 year: 2012 ident: D3CC02512H/cit23/1 publication-title: Organometallics doi: 10.1021/om3003762 – volume: 129 start-page: 12049 year: 2007 ident: D3CC02512H/cit2b/1 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja074019e – volume: 54 start-page: 7597 year: 2015 ident: D3CC02512H/cit10a/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201502531 – volume: 90 start-page: 191 year: 1990 ident: D3CC02512H/cit8a/1 publication-title: Chem. Rev. doi: 10.1021/cr00099a007 – volume: 57 start-page: 16968 year: 2018 ident: D3CC02512H/cit8c/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201803888 – volume: 5 start-page: 7375 year: 2017 ident: D3CC02512H/cit18c/1 publication-title: J. Mater. Chem. C doi: 10.1039/C7TC02511D – volume: 43 start-page: 6250 year: 2004 ident: D3CC02512H/cit17a/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.200400655 – volume: 46 start-page: 444 year: 2013 ident: D3CC02512H/cit3c/1 publication-title: Acc. Chem. Res. doi: 10.1021/ar300196u – volume: 133 start-page: 2868 year: 2011 ident: D3CC02512H/cit15/1 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja200462y – start-page: 191 year: 1981 ident: WOS:A1981LD16900032 article-title: A SOLID SILAETHENE - ISOLATION AND CHARACTERIZATION publication-title: JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS – volume: 2 start-page: 678 year: 2023 ident: WOS:001124816600001 article-title: A class of non-aromatic 1,3-disilapyrroles acting as stable organosilicon-based triplet diradicals publication-title: NATURE SYNTHESIS doi: 10.1038/s44160-023-00279-6 – volume: 31 start-page: 4588 year: 2012 ident: WOS:000305588000026 article-title: Facile Access to the Functionalized N-Donor Stabilized Silylenes PhC(NtBu)2SiX (X = PPh2, NPh2, NCy2, NiPr2, NMe2, N(SiMe3)2, OtBu) publication-title: ORGANOMETALLICS doi: 10.1021/om3003762 – volume: 45 start-page: 3948 year: 2006 ident: WOS:000238501500010 article-title: Synthesis and characterization of [PhC(NtBu)2]SiCl:: A stable monomeric chlorosilylene publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200600647 – volume: 60 start-page: 7143 year: 2021 ident: WOS:000653539100037 article-title: Si(II) Cation-Promoted Formation of an Abnormal NHC-Bound Silylene and a cAAC-Silanyl Radical Ion publication-title: INORGANIC CHEMISTRY doi: 10.1021/acs.inorgchem.1c00188 – volume: 50 start-page: 2322 year: 2011 ident: WOS:000288036300021 article-title: Zwitterionic Si-C-Si-P and Si-P-Si-P Four-Membered Rings with Two-Coordinate Phosphorus Atoms publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201005866 – volume: 46 start-page: 5873 year: 2010 ident: WOS:000280658300007 article-title: Synthesis, structure, and theoretical investigation of amidinato supported 1,4-disilabenzene publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c0cc01753a – volume: 48 start-page: 14242 year: 2019 ident: WOS:000488472000004 article-title: Oligomerization of phosphaalkynes mediated by bulky N-heterocyclic carbenes: avenues to novel phosphorus frameworks publication-title: DALTON TRANSACTIONS doi: 10.1039/c9dt03185e – volume: 61 start-page: 15864 year: 2022 ident: WOS:000920930200001 article-title: Isolation of Silacycles from the Reactions of a Monochlorosilylene LSi(:)Cl (L = PhC(NtBu)2) with Ethynyl Lithium Salts publication-title: INORGANIC CHEMISTRY doi: 10.1021/acs.inorgchem.2c01762 – volume: 28 start-page: ARTN e202201963 year: 2022 ident: WOS:000835372600001 article-title: Stereoselective Activation of Small Molecules by a Stable Chiral Silene publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.202201963 – volume: 61 start-page: ARTN e202114598 year: 2022 ident: WOS:000753976500003 article-title: Deoxygenation of Nitrous Oxide and Nitro Compounds Using Bis(N-Heterocyclic Silylene)Amido Iron Complexes as Catalysts publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.202114598 – volume: 104 start-page: 5667 year: 1982 ident: WOS:A1982PL96900019 article-title: STABLE SOLID SILAETHYLENES publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY – volume: 132 start-page: 1123 year: 2010 ident: WOS:000275084700041 article-title: High Yield Access to Silylene RSiCl (R = PhC(NtBu)2) and Its Reactivity toward Alkyne: Synthesis of Stable Disilacyclobutene publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja9091374 – volume: 244 start-page: 1 year: 2003 ident: WOS:000186381800001 article-title: Linear organic π-conjugated systems featuring the heavy Group 14 and 15 elements publication-title: COORDINATION CHEMISTRY REVIEWS doi: 10.1016/S0010-8545(03)00098-5 – volume: 144 start-page: 22446 year: 2022 ident: WOS:000898842500001 article-title: Neutral Homoaromatic Diboradisilacyclobutene: Synthesis, Structure, and Reactivity publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.2c11204 – volume: 111 start-page: 354 year: 2011 ident: WOS:000287620600004 article-title: N-Heterocyclic Carbene Analogues with Low-Valent Group 13 and Group 14 Elements: Syntheses, Structures, and Reactivities of a New Generation of Multitalented Ligands publication-title: CHEMICAL REVIEWS doi: 10.1021/cr100216y – volume: 50 start-page: 12510 year: 2011 ident: WOS:000298332700014 article-title: A Stable Cation of a CSi3P Five-Membered Ring with a Weakly Coordinating Chloride Anion publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201104146 – volume: 4 start-page: 113 year: 2003 ident: WOS:000186977000008 article-title: High efficiency molecular organic light-emitting diodes based on silole derivatives and their exciplexes publication-title: ORGANIC ELECTRONICS doi: 10.1016/j.orgel.2003.08.006 – volume: 34 start-page: 164 year: 2005 ident: WOS:000226522500006 article-title: Microwaves in organic synthesis.: Thermal and non-thermal microwave effects publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/b411438h – volume: 58 start-page: 273 year: 2019 ident: WOS:000455818400041 article-title: Facile Cleavage of the P=P Double Bond in Vinyl-Substituted Diphosphenes publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201812592 – volume: 39 start-page: 4282 year: 2020 ident: WOS:000599997800025 article-title: A C2-Linked Bis-silene Formed without Using Metals and the Transformation into the Bis-silyl and Bis-silylium C4-Cumulenes publication-title: ORGANOMETALLICS doi: 10.1021/acs.organomet.0c00368 – volume: 90 start-page: 191 year: 1990 ident: WOS:A1990CP98500008 article-title: UNUSUALLY COORDINATED PHOSPHORUS-COMPOUNDS .41. PHOSPHAALKYNES - NEW BUILDING-BLOCKS IN SYNTHETIC CHEMISTRY publication-title: CHEMICAL REVIEWS – volume: 54 start-page: 7597 year: 2015 ident: WOS:000356390900024 article-title: Synthesis of Phosphabenzenes by an Iron-Catalyzed [2+2+2] Cycloaddition Reaction of Diynes with Phosphaalkynes publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201502531 – volume: 22 start-page: 432 year: 2011 ident: WOS:000291910600023 article-title: Addition of a Stable Dialkylsilylene to Carbon-Carbon Unsaturated Bonds publication-title: HETEROATOM CHEMISTRY doi: 10.1002/hc.20705 – volume: 9 start-page: 236 year: 2009 ident: WOS:000271136800003 article-title: Organophosphine Syntheses via Activation of the Phosphorus-Silicon Bond of Silylphosphines publication-title: CHEMICAL RECORD doi: 10.1002/tcr.200900011 – volume: 46 start-page: 444 year: 2013 ident: WOS:000315478700024 article-title: Dichlorosilylene: A High Temperature Transient Species to an Indispensable Building Block publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar300196u – volume: 132 start-page: 12841 year: 2010 ident: WOS:000282013700028 article-title: Diastereoselective Synthesis of Bulky, Strongly Nucleophilic, and Configurationally Stable P-Stereogenic Tricyclic Phosphines publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja1054912 – volume: 59 start-page: 23015 year: 2020 ident: WOS:000579476500001 article-title: A Neutral Three-Membered 2π Aromatic Disilaborirane and the Unique Conversion into a Four-Membered BSi2N-Ring publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.202009638 – volume: 49 start-page: 6733 year: 2020 ident: WOS:000571350600010 article-title: Where silylene-silicon centres matter in the activation of small molecules publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/d0cs00815j – volume: 133 start-page: 12311 year: 2011 ident: WOS:000293768400077 article-title: Striking Stability of a Substituted Silicon(II) Bis(trimethylsilyl)amide and the Facile Si-Me Bond Cleavage without a Transition Metal Catalyst publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja205369h – volume: 51 start-page: 7158 year: 2012 ident: WOS:000306314300016 article-title: Synthesis and Characterization of an Isolable Base-Stabilized Silacycloprop-1-ylidene publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201201581 – volume: 133 start-page: 2868 year: 2011 ident: WOS:000289455200020 article-title: An Ylide-like Phosphasilene and Striking Formation of a 4π-Electron, Resonance-Stabilized 2,4-Disila-1,3-diphosphacyclobutadiene publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja200462y – volume: 33 start-page: 813 year: 2000 ident: WOS:000165603800009 article-title: Development of reactions of silacyclopropanes as new methods for stereoselective organic synthesis publication-title: ACCOUNTS OF CHEMICAL RESEARCH – volume: 39 start-page: 2307 year: 2000 ident: WOS:000088181900020 article-title: Novel 1,2,4-triphosphole and 1,2,3-triphosphetene derivatives from N,N′-bis(2,2-dimethylpropyl)benzimidazolin-2-ylidene and phosphaalkynes publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION – volume: 16 start-page: 12956 year: 2010 ident: WOS:000284063900026 article-title: Synthesis and Characterization of an Amidinate-Stabilized cis-1,2-Disilylenylethene [cis-LSi{C(Ph)=C(H)}SiL] and a Singlet Delocalized Biradicaloid [LSi(μ2-C2Ph2)2SiL] publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201001141 – volume: 129 start-page: 12049 year: 2007 ident: WOS:000249887700037 article-title: Synthesis and structures of heteroleptic silylenes publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja074019e – volume: 270 start-page: 57 year: 2014 ident: WOS:000336013800005 article-title: Main group and transition metal-mediated phosphaalkyne oligomerizations publication-title: COORDINATION CHEMISTRY REVIEWS doi: 10.1016/j.ccr.2013.10.005 – volume: 62 start-page: 1095 year: 2023 ident: WOS:000914746700001 article-title: Diverse Reactions of o-Carborane-Fused Silylenes with CE (E = C, P) Triple Bonds publication-title: INORGANIC CHEMISTRY doi: 10.1021/acs.inorgchem.2c03140 – volume: 50 start-page: 12753 year: 2014 ident: WOS:000342990400040 article-title: Bypassing a highly unstable frustrated Lewis pair: dihydrogen cleavage by a thermally robust silylium-phosphine adduct publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c4cc05905k – volume: 73 start-page: 895 year: 2018 ident: WOS:000448777600018 article-title: Functionalization of 1,3-diphosphacyclobutadiene cobalt complexes via Si-P bond insertion publication-title: ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES doi: 10.1515/znb-2018-0121 – volume: 16 start-page: 4133 year: 2006 ident: WOS:000241516700008 article-title: Poly(3,6-silafluorene-co-2,7-fluorene)-based high-efficiency and color-pure blue light-emitting polymers with extremely narrow band-width and high spectral stability publication-title: JOURNAL OF MATERIALS CHEMISTRY doi: 10.1039/b609250k – start-page: 1929 year: 2007 ident: WOS:000246312000011 article-title: Differing reactivities of PCMe and PCBut towards a triphosphabenzene and a tetraphosphabarrelene:: synthesis of new phosphaalkyne pentamers (P5C5MenBut5-n, n=0, 1 or 2) publication-title: DALTON TRANSACTIONS doi: 10.1039/b618515k – volume: 5 start-page: 7375 year: 2017 ident: WOS:000406848400001 article-title: Siloles in optoelectronic devices publication-title: JOURNAL OF MATERIALS CHEMISTRY C doi: 10.1039/c7tc02511d – volume: 43 start-page: 6250 year: 2004 ident: WOS:000225575600006 article-title: Controlled microwave heating in modern organic synthesis publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200400655 – volume: 58 start-page: 3715 year: 2019 ident: WOS:000462680700006 article-title: Isolable Silylene Ligands Can Boost Efficiencies and Selectivities in Metal-Mediated Catalysis publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201811088 – volume: 57 start-page: 16968 year: 2018 ident: WOS:000454575500006 article-title: The Chemistry of the 2-Phosphaethynolate Anion publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201803888 |
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| Snippet | 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... Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArCCR (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... Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArC CR (Ar = Ph, 4-iPr-C6H4, 3-F-C6H4; R = H, Ph) at 80 degrees C under microwave irradiation to afford... Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArCCR (Ar = Ph, 4-iPr-C H , 3-F-C H ; R = H, Ph) at 80 °C under microwave irradiation to afford... Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArC≡CR (Ar = Ph, 4-iPr-C6H4, 3-F-C6H4; R = H, Ph) at 80 °C under microwave irradiation to afford... Bis(1-adamantyl)phosphanylsilylene 1 was reacted with ArCCR (Ar = Ph, 4-iPr-C6H4, 3-F-C6H4; R = H, Ph) at 80 °C under microwave irradiation to afford... |
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| Title | SiP-heterocycles derived from a bulky phosphanylsilylene |
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