In:
Chemistry – A European Journal, Wiley, Vol. 24, No. 19 ( 2018-04-03), p. 4967-4972
Kurzfassung:
Compared with the well‐known anion‐templated effects in shaping silver thiolate clusters, the influence from the organic ligands in the outer shell is still poorly understood. Herein, three new benzoate‐functionalized high‐nuclearity silver(I) thiolate clusters are isolated and characterized for the first time in the presence of diverse anion templates such as S 2− , α‐[Mo 5 O 18 ] 6− , and MoO 4 2− . Single‐crystal X‐ray analysis reveals that the nuclearities of the three silver clusters ( SD/Ag28 , SD/Ag29 , SD/Ag30 ) vary from 32 to 38 to 78 with co‐capped t BuS − and benzoate ligands on the surface. SD/Ag28 is a turtle‐like cluster comprising a Ag 29 shell caging a Ag 3 S 3 trigon in the center, whereas SD/Ag29 is a prolate Ag 38 sphere templated by the α‐[Mo 5 O 18 ] 6− anion. Upon changing from benzoate to methoxyl‐substituted benzoate, SD/Ag30 is isolated as a very complicated core–shell spherical cluster composed of a Ag 57 shell and a vase‐like Ag 21 S 13 core. Four MoO 4 2− anions are arranged in a supertetrahedron and located in the interstice between the core and shell. Introduction of the bulky benzoate changes elaborately the nuclearity and arrangements of silver polygons on the shell of silver clusters, which is exemplified by comparing SD/Ag28 and a known similar silver thiolate cluster. The three new clusters emit luminescence in the near‐infrared (NIR) region and show different thermochromic luminescence properties. This work presents a flexible approach to synthetic studies of high‐nuclearity silver clusters decorated by different benzoates, and structural modulations are also achieved.
Materialart:
Online-Ressource
ISSN:
0947-6539
,
1521-3765
DOI:
10.1002/chem.201800007
Sprache:
Englisch
Verlag:
Wiley
Publikationsdatum:
2018
ZDB Id:
1478547-X
