Literature DB >> 12375942

1,1',3,3',6,6',8,8'-Octachloro-9,9'-bifluorenylidene and perchloro-9,9'-bifluorenylidene, two exceedingly twisted ethylenes.

Elies Molins1, Carlos Miravitlles, Enrique Espinosa, Manuel Ballester.   

Abstract

The syntheses of 1,1',3,3',6,6',8,8'-octachloro-9,9'-bifluorenylidene (1), its precursors, and the byproduct 3,3',5,5'-tetrachloro-4-(trichloromethyl)biphenyl (5) are described. Accurate structural X-ray data on 1 and on perchloro-9,9'-bifluorenylidene (2) are reported and discussed. Because of chlorine overcrowding, the dihedral angles between their two identical fluorenylidene moieties are abnormally large, the central-ethylene twist angles being 55 and 66 degrees, respectively. Significant out-of-plane carbon-chlorine bond bending is likewise exhibited. Their ESR spectra and magnetic measurements prove that they are singlet species. The exceptionally large bathochromic displacements of their UV-vis absorption spectrum with respect to that of their parent hydrocarbon are mainly attributed to bond bending and molecular warping.

Entities:  

Year:  2002        PMID: 12375942     DOI: 10.1021/jo010979m

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Bis-dibenzo[a.i]fluorenylidene, does it exist as stable 1,2-diradical?

Authors:  Basem Kanawati; Alexander Genest; Philippe Schmitt-Kopplin; Dieter Lenoir
Journal:  J Mol Model       Date:  2012-07-03       Impact factor: 1.810

2.  2-Azido-1-(3,6-dichloro-9H-fluoren-1-yl)ethanone.

Authors:  Hoong-Kun Fun; Tze Shyang Chia; Reshma Kayarmar; G K Nagaraja
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-09-17

3.  Isolation of diborenes and their 90°-twisted diradical congeners.

Authors:  Julian Böhnke; Theresa Dellermann; Mehmet Ali Celik; Ivo Krummenacher; Rian D Dewhurst; Serhiy Demeshko; William C Ewing; Kai Hammond; Merlin Heß; Eckhard Bill; Eileen Welz; Merle I S Röhr; Roland Mitrić; Bernd Engels; Franc Meyer; Holger Braunschweig
Journal:  Nat Commun       Date:  2018-03-22       Impact factor: 14.919

  3 in total

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