Novel conformational isomerism in a six-coordinate silver(i) complex of a sexadentate macrocycle with an 'N3S3' donor set
The synthesis and structural characterization of the condensation product formed by a template reaction of 2, 6-diacetylpyridine and 3, 6, 9-trithiaundecane-1, 11-diamine about silver(1) (as perchlorate) are described. Crystals are monoclinic, C2/c, a 27.114(10), b 7.546(5), c 22.137(10) Å, β 105.35...
Saved in:
| Main Authors: | , , |
|---|---|
| Format: | Article |
| Published: |
CSIRO Publishing
1989
|
| Online Access: | http://psasir.upm.edu.my/id/eprint/115194/ https://www.publish.csiro.au/ch/CH9891387 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | The synthesis and structural characterization of the condensation product formed by a template reaction of 2, 6-diacetylpyridine and 3, 6, 9-trithiaundecane-1, 11-diamine about silver(1) (as perchlorate) are described. Crystals are monoclinic, C2/c, a 27.114(10), b 7.546(5), c 22.137(10) Å, β 105.35(3)°, Z=8×[AgL]+(ClO4)- (L = C17H25N3S3). R was 0.057 for 2372 'observed' reflections. The six-coordinate silver(l) atom lies in a novel environment comprised of a mer-triaza moiety derived from 2, 6-diacetylpyridine [Ag-N, 2.422(8) (central), 2.538(8), 2.546(9) Å (distal)] and a fac-trithia moiety straddling its plane [Ag-S, 2.603(6) (central), 2-815(4), 2.881(3) Å (distal)]. The complex cation is a different conformational isomer to that found in the previously studied tetraphenylborate salt. In the latter, Ag-N are 2.422(9) (central), 2.613(9), 2.399(7) Å (distal), with Ag-S 2.670(3) (central), 2.655(3), 2.949(4) Å (distal). |
|---|