Literature DB >> 19787856

Ultrafast UV-visible and infrared spectroscopic observation of a singlet vinylcarbene and the intramolecular cyclopropenation reaction.

Yunlong Zhang1, Jacek Kubicki, Matthew S Platz.   

Abstract

Ultrafast UV-vis/IR spectroscopies were used to study the photochemistry of a vinyl diazo ester PhCH=CHCN2CO2CH3 (1) in solution. The results indicate that singlet styrylcarbomethoxy carbene ((1)2) is produced from the excited state of diazo precursor (1*). It is concluded that vinyl singlet carbene ((1)2) undergoes an intramolecular cyclopropenation reaction to produce the cyclopropene product (3), and undergoes intersystem crossing to ground triplet carbene ((3)2). The predictions of DFT calculations are consistent with the observations.

Entities:  

Year:  2009        PMID: 19787856     DOI: 10.1021/ja905992p

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  3 in total

1.  Diamidocarbenes as versatile and reversible [2 + 1] cycloaddition reagents.

Authors:  Jonathan P Moerdyk; Christopher W Bielawski
Journal:  Nat Chem       Date:  2012-02-12       Impact factor: 24.427

2.  Combined In Situ Illumination-NMR-UV/Vis Spectroscopy: A New Mechanistic Tool in Photochemistry.

Authors:  Andreas Seegerer; Philipp Nitschke; Ruth M Gschwind
Journal:  Angew Chem Int Ed Engl       Date:  2018-03-30       Impact factor: 15.336

3.  Photochemical ring expansion reactions: synthesis of tetrahydrofuran derivatives and mechanism studies.

Authors:  Sripati Jana; Zhen Yang; Chao Pei; Xinfang Xu; Rene M Koenigs
Journal:  Chem Sci       Date:  2019-09-06       Impact factor: 9.825

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.