Equilibrium Formation of Stable All-Silicon Versions of 1,3-Cyclobutanediyl.
diradicaloids
low-valent species
silicon
small ring
synthesis
Journal
Angewandte Chemie (International ed. in English)
ISSN: 1521-3773
Titre abrégé: Angew Chem Int Ed Engl
Pays: Germany
ID NLM: 0370543
Informations de publication
Date de publication:
24 Aug 2020
24 Aug 2020
Historique:
received:
30
04
2020
pubmed:
15
5
2020
medline:
15
5
2020
entrez:
15
5
2020
Statut:
ppublish
Résumé
Main group analogues of cyclobutane-1,3-diyls are fascinating due to their unique reactivity and electronic properties. So far only heteronuclear examples have been isolated. Here we report the isolation and characterization of all-silicon 1,3-cyclobutanediyls as stable closed-shell singlet species from the reversible reactions of cyclotrisilene c-Si
Identifiants
pubmed: 32407571
doi: 10.1002/anie.202006283
pmc: PMC7496386
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
15087-15092Subventions
Organisme : Deutscher Akademischer Austauschdienst
Organisme : Türkiye Bilimsel ve Teknolojik Araştirma Kurumu
ID : 2214-A
Informations de copyright
© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
Références
J Am Chem Soc. 2011 Aug 17;133(32):12478-81
pubmed: 21776998
Angew Chem Int Ed Engl. 2015 Jan 7;54(2):668-72
pubmed: 25404061
Chemistry. 2014 Jul 21;20(30):9221-4
pubmed: 24827791
Angew Chem Int Ed Engl. 2013 Feb 11;52(7):2105-8
pubmed: 23319315
Angew Chem Int Ed Engl. 2013 Jan 2;52(1):450-4
pubmed: 23169591
Nat Chem. 2013 Oct;5(10):876-9
pubmed: 24056345
Angew Chem Int Ed Engl. 2020 Aug 24;59(35):15087-15092
pubmed: 32407571
J Magn Reson. 2006 Jan;178(1):42-55
pubmed: 16188474
Angew Chem Int Ed Engl. 2011 Sep 12;50(38):8974-8
pubmed: 21858902
J Am Chem Soc. 2017 Sep 27;139(38):13499-13506
pubmed: 28856886
J Am Chem Soc. 2002 Jun 12;124(23):6540-1
pubmed: 12047167
Chem Soc Rev. 2012 Jan 7;41(1):303-49
pubmed: 21850355
Chem Soc Rev. 2016 Feb 21;45(4):1080-111
pubmed: 26585359
J Am Chem Soc. 2019 Aug 14;141(32):12916-12927
pubmed: 31337219
Angew Chem Int Ed Engl. 2012 Jul 2;51(27):6785-8
pubmed: 22639373
Chem Rev. 2013 Sep 11;113(9):7011-88
pubmed: 23883325
Science. 2002 Mar 8;295(5561):1880-1
pubmed: 11884750
Angew Chem Int Ed Engl. 2016 Oct 4;55(41):12868-72
pubmed: 27628158
Proc Jpn Acad Ser B Phys Biol Sci. 2012;88(5):167-91
pubmed: 22687739
Angew Chem Int Ed Engl. 2004 Aug 27;43(34):4500-4
pubmed: 15340953
Angew Chem Int Ed Engl. 2016 Feb 18;55(8):2907-10
pubmed: 26800440
Angew Chem Int Ed Engl. 2004 Feb 1;43(5):585-7
pubmed: 14743410
J Am Chem Soc. 2010 Aug 4;132(30):10264-5
pubmed: 20662508
J Am Chem Soc. 2011 Apr 20;133(15):5773-5
pubmed: 21443193
Chem Soc Rev. 2018 Apr 23;47(8):2534-2553
pubmed: 29498718
Angew Chem Int Ed Engl. 2018 Feb 23;57(9):2445-2449
pubmed: 29316108
Angew Chem Int Ed Engl. 2015 Oct 5;54(41):12144-8
pubmed: 26297814
Chem Rev. 2019 Nov 13;119(21):11291-11351
pubmed: 31593450
Angew Chem Int Ed Engl. 2013 Dec 9;52(50):13247-50
pubmed: 24307015
Angew Chem Int Ed Engl. 2011 Aug 16;50(34):7936-9
pubmed: 21728221
J Am Chem Soc. 2004 Jun 2;126(21):6510-1
pubmed: 15161252
Chem Rev. 2003 Mar;103(3):789-810
pubmed: 12630853
Chem Commun (Camb). 2020 Jan 16;56(5):747-750
pubmed: 31845675
Angew Chem Int Ed Engl. 2015 Jan 7;54(2):683-6
pubmed: 25418506
J Phys Chem Lett. 2017 Apr 6;8(7):1677-1682
pubmed: 28345918
Front Chem. 2019 Feb 01;7:10
pubmed: 30775359
J Am Chem Soc. 2020 Jun 3;142(22):9920-9924
pubmed: 32375476
Chemistry. 2012 Apr 2;18(14):4258-63
pubmed: 22378245
Chem Soc Rev. 2015 Sep 21;44(18):6578-96
pubmed: 25994857
Chem Soc Rev. 2012 May 21;41(10):3808-20
pubmed: 22377794