Spin Crossover in a Series of Non-Hofmann-Type Fe(II) Coordination Polymers Based on [Hg(SeCN)3]- or [Hg(SeCN)4]2- Building Blocks.
Inorg Chem
; 60(15): 11048-11057, 2021 Aug 02.
Article
in En
| MEDLINE
| ID: mdl-34279097
ABSTRACT
Self-assembly of [Hg(SeCN)4]2- tetrahedral building blocks, iron(II) ions, and a series of bis-monodentate pyridyl-type bridging ligands has afforded the new heterobimetallic HgII-FeII coordination polymers {Fe[Hg(SeCN)3]2(4,4'-bipy)2}n (1), {Fe[Hg(SeCN)4](tvp)}n (2), {Fe[Hg(SeCN)3]2(4,4'-azpy)2}n (3), {Fe[Hg(SeCN)4](4,4'-azpy)(MeOH)}n (4), {Fe[Hg(SeCN)4](3,3'-bipy)}n (5) and {Fe[Hg(SeCN)4](3,3'-azpy)}n (6) (4,4-bipy = 4,4'-bipyridine, tvp = trans-1,2-bis(4-pyridyl)ethylene, 4,4'-azpy = 4,4'-azobispyridine, 3,3-bipy = 3,3'-bipyridine, 3,3'-azpy = 3,3'-azobispyridine). Single-crystal X-ray analyses show that compounds 1 and 3 display a two-dimensional robust sheet structure made up of infinite linear [(FeL)n]2n+ (L = 4,4'-bipy or 4,4'-azpy) chains linked by in situ formed {[Hg(L)(SeCN)3]2}2- anionic dimeric bridges. Complexes 2 and 4-6 define three-dimensional networks with different topological structures, indicating, in combination with complexes 1 and 3, that the polarity, length, rigidity, and conformation of the bridging organic ligand play important roles in the structural nature of the products reported here. The magnetic properties of complexes 1 and 2 show the occurrence of temperature- and light-induced spin crossover (SCO) properties, while complexes 4-6 are in the high-spin state at all temperatures. The current results provide a new route for the design and synthesis of new SCO functional materials with non-Hofmann-type traditional structures.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Language:
En
Journal:
Inorg Chem
Year:
2021
Document type:
Article