CROWN-ETHER ANNELATED TETRATHIAFULVALENES .2.

被引:53
作者
HANSEN, TK
JORGENSEN, T
JENSEN, F
THYGESEN, PH
CHRISTIANSEN, K
HURSTHOUSE, MB
HARMAN, ME
MALIK, MA
GIRMAY, B
UNDERHILL, AE
BEGTRUP, M
KILBURN, JD
BELMORE, K
ROEPSTORFF, P
BECHER, J
机构
[1] SCH CHEM & APPL CHEM,CARDIFF GF1 3TB,WALES
[2] UNIV COLL N WALES,DEPT CHEM,BANGOR LL57 2UW,GWYNEDD,WALES
[3] DANISH FARMACEUT UNIV,DK-2100 COPENHAGEN,DENMARK
[4] UNIV SOUTHAMPTON,DEPT CHEM,SOUTHAMPTON SO9 5NH,HANTS,ENGLAND
[5] UNIV ALABAMA,DEPT CHEM,TUSCALOOSA,AL 35487
[6] ODENSE UNIV,DEPT MOLEC BIOL,DK-5230 ODENSE,DENMARK
关键词
D O I
10.1021/jo00058a013
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A synthetic procedure leading to derivatives of tetrathiafulvalene (TTF) incorporating polyether chains of various lengths, some nitrogen analogs, and a 2,6-bis(methylene)pyridine analog has been developed. These compounds possess cage-type structures which were confirmed by X-ray crystallography in four cases, two of which are reported herein for the first time. Structural and electronic features of these cage molecules were correlated to oxidation potentials by the use of semiempirical methods (MNDO-PM3). An investigation of the alkali metal ion affinity using PDMS revealed that these compounds are poor ligands. Finally, in one case, protonation of the core TTF was studied by NMR.
引用
收藏
页码:1359 / 1366
页数:8
相关论文
共 33 条