Matches in SemOpenAlex for { <https://semopenalex.org/work/W2007507965> ?p ?o ?g. }
Showing items 1 to 52 of
52
with 100 items per page.
- W2007507965 endingPage "1474" @default.
- W2007507965 startingPage "1471" @default.
- W2007507965 abstract "PA, C18H14C12N20282, Mr=425.36, tri- clinic, P1 (after structure determination), a-- 11.232(2), b=10.465(2), c=8.386(2) A, a= 107-07 (3), fl = 83-63 (4), y = 98.90 (3) °, V= 928.7 (4)/~3, Z = 2, Dx = 1.521 g cm -3, ,~(Mo Ka) = 0.71069 A,/1, = 5.27 cm -~, F(000)= 436, room tem- perature. Final conventional R value is 0.033 (wR = 0.041) for 2716 diffractometer-measured intensities with I___ 3tr(l). The molecular structure is charac- terized by the different conformations of the two thiazolidine rings, one of which is an envelope, and by opposite chirality of the two asymmetric C atoms. In the crystal structure both the enantiomers 2S,2'R and 2R,2'S are present. PB, CI8HI4C12N20282, Mr = 425.36, orthorhombic, Pbcn, a=7.759(2), b= 19.625 (4), c = 12.504 (3) A, V= 1904.0 (6) A 3, Z = 4, Dx = 1.483 g cm -3, a(Mo Ka) = 0.71069 A, /1, = 5.14cm -I, F(000)= 872, room temperature. Final conventional R value is 0.049 (wR = 0.067) for 1334 diffractometer-measured intensities with I_> 3tr(l). Because the molecular structure has exact C2 sym- metry, the two phenyl rings are strictly parallel and the conformations (half chair) of the two thiazolidine rings are the same as well as the chirality of the two asymmetric C atoms. Nevertheless both enantiomers 2R,2R and 2S,2S are in the crystal." @default.
- W2007507965 created "2016-06-24" @default.
- W2007507965 creator A5008377457 @default.
- W2007507965 creator A5053046369 @default.
- W2007507965 creator A5059551658 @default.
- W2007507965 creator A5061234792 @default.
- W2007507965 creator A5065202591 @default.
- W2007507965 creator A5073443868 @default.
- W2007507965 date "1990-08-15" @default.
- W2007507965 modified "2023-09-23" @default.
- W2007507965 title "Structures of the configurational isomers of 2,2'-bis(3-chlorophenyl)[3,3'-bi-1,3-thiazolidine]-4,4'-dione" @default.
- W2007507965 doi "https://doi.org/10.1107/s0108270189012503" @default.
- W2007507965 hasPublicationYear "1990" @default.
- W2007507965 type Work @default.
- W2007507965 sameAs 2007507965 @default.
- W2007507965 citedByCount "1" @default.
- W2007507965 crossrefType "journal-article" @default.
- W2007507965 hasAuthorship W2007507965A5008377457 @default.
- W2007507965 hasAuthorship W2007507965A5053046369 @default.
- W2007507965 hasAuthorship W2007507965A5059551658 @default.
- W2007507965 hasAuthorship W2007507965A5061234792 @default.
- W2007507965 hasAuthorship W2007507965A5065202591 @default.
- W2007507965 hasAuthorship W2007507965A5073443868 @default.
- W2007507965 hasConcept C147597530 @default.
- W2007507965 hasConcept C185592680 @default.
- W2007507965 hasConcept C2776590680 @default.
- W2007507965 hasConcept C71240020 @default.
- W2007507965 hasConceptScore W2007507965C147597530 @default.
- W2007507965 hasConceptScore W2007507965C185592680 @default.
- W2007507965 hasConceptScore W2007507965C2776590680 @default.
- W2007507965 hasConceptScore W2007507965C71240020 @default.
- W2007507965 hasIssue "8" @default.
- W2007507965 hasLocation W20075079651 @default.
- W2007507965 hasOpenAccess W2007507965 @default.
- W2007507965 hasPrimaryLocation W20075079651 @default.
- W2007507965 hasRelatedWork W2016865072 @default.
- W2007507965 hasRelatedWork W2093861474 @default.
- W2007507965 hasRelatedWork W2094270034 @default.
- W2007507965 hasRelatedWork W2094479206 @default.
- W2007507965 hasRelatedWork W2146153230 @default.
- W2007507965 hasRelatedWork W2149055735 @default.
- W2007507965 hasRelatedWork W2342802239 @default.
- W2007507965 hasRelatedWork W2355332489 @default.
- W2007507965 hasRelatedWork W2365149494 @default.
- W2007507965 hasRelatedWork W2953195768 @default.
- W2007507965 hasVolume "46" @default.
- W2007507965 isParatext "false" @default.
- W2007507965 isRetracted "false" @default.
- W2007507965 magId "2007507965" @default.
- W2007507965 workType "article" @default.