The dimer, trimer and 1,2,4‐trithiolane of adamantanethione
Author(s) -
Linden Anthony,
Fu Changchun,
Majchrzak Agnieszka,
Mloston Grzegorz,
Heimgartner Heinz
Publication year - 2002
Publication title -
acta crystallographica section c
Language(s) - English
Resource type - Journals
eISSN - 1600-5759
pISSN - 0108-2701
DOI - 10.1107/s0108270102003190
Subject(s) - trimer , dimer , chemistry , d dimer , medicine , organic chemistry , gastroenterology
The molecules of dispiro[1,3‐dithietane‐2,2′:4,2′′‐diadamantane], C 20 H 28 S 2 , have crystallographic C i symmetry, as well as local D 2 h symmetry, and a planar 1,3‐dithietane ring. The molecules of trispiro[1,3,5‐trithiane‐2,2′:4,2′′:6,2′′′‐triadamantane], C 30 H 42 S 3 , have approximate C 2 symmetry and the 1,3,5‐trithiane ring has a twist–boat conformation. The C—S—C bond angles within the ring are about 8° larger than observed in most related 1,3,5‐trithiane structures. In dispiro[1,2,4‐trithiolane‐3,2′:5,2′′‐diadamantane], C 20 H 28 S 3 , the molecules have local C 2 symmetry and the 1,2,4‐trithiolane ring has a half‐chair conformation.
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