SYNTHESIS, STRUCTURE AND PROPERTIES OF VARIOUS MOLECULES BASED ON THE2-TRIOXA-4,8,12,12C-TETRAHYDRODIBENZO[CD,MN]PYRENE SYSTEM WITH AN EVALUATION OF THE EFFECT DIFFERING MOLECULAR SUBSTITUTION PATTERNS HAS ONTHE SPACE GROUP SYMMETRY

Citation
A. Faldt et al., SYNTHESIS, STRUCTURE AND PROPERTIES OF VARIOUS MOLECULES BASED ON THE2-TRIOXA-4,8,12,12C-TETRAHYDRODIBENZO[CD,MN]PYRENE SYSTEM WITH AN EVALUATION OF THE EFFECT DIFFERING MOLECULAR SUBSTITUTION PATTERNS HAS ONTHE SPACE GROUP SYMMETRY, Perkin transactions. 2, (11), 1997, pp. 2219-2227
Citations number
30
Categorie Soggetti
Chemistry Physical","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
03009580
Issue
11
Year of publication
1997
Pages
2219 - 2227
Database
ISI
SICI code
0300-9580(1997):11<2219:SSAPOV>2.0.ZU;2-9
Abstract
2-Trioxa-4,8,12,12c-tetrahydrodibenzo[cd,mn]pyrene (3), t-butyl-4,8,12 -trioxa-4,8,12,12c-tetrahydrodibenzo [cd,mn]pyrene (11) and tri-tert-b utyl-4,8,12-trioxa-12c-methyl-4,8,12,12c -tetrahydrodibenzo[cd,mn]pyre ne (12) have been synthesised and their crystal structures determined, The crystal structure of ophospha-4,8,12,12c-tetrahydrodibenzo[cd,mn] pyrene (13) has also been determined for comparison, Compounds 3 and 1 1 crystallise in non-centrosymmetric space groups, Compound 12 also cr ystallises in a non-centrosymmetric :space group but molecules of oppo site chirality are present within the unit cell, Finally compound 13 c rystallises in a centrosymmetric space group, The room temperature pyr oelectric coefficient of 3 has been determined, The spatial extent of the trioxatriangulene ground system has been perturbed by chemical sub stitution and the effect: of the substitutions upon the space group sy mmetry of the chemical derivative has been uncovered by X-ray structur al resolution, The non-centrosymmetric point group symmetry of the mol ecules is reflected in a non-centrosymmetric space group symmetry when ever the spatial perturbations do not prohibit the stacking of the mol ecules.