| Literature DB >> 29111697 |
Yuxiang Chen1, Fang Ma2, Xiaoxiang Chen3, Bowei Dong3, Kang Wang1, Shangda Jiang3, Chiming Wang1, Xin Chen1, Dongdong Qi1, Haoling Sun2, Bingwu Wang3, Song Gao3, Jianzhuang Jiang1.
Abstract
Bulky and strong electron-donating dibutylamino groups were incorporated onto the peripheral positions of one of the two phthalocyanine ligands in the bis(phthalocyaninato) terbium complex, resulting in the isolation of heteroleptic double-decker (Pc)Tb{Pc[N(C4H9)2]8} {Pc = phthalocyaninate; Pc[N(C4H9)2]8 = 2,3,9,10,16,17,23,24-octakis(dibutylamino)phthalocyaninate} with the nature of an unsymmetrical molecular structure, a square-antiprismatic coordination geometry, an intensified coordination field strength, and the presence of organic radical-f interaction. As a total result of all these factors, this sandwich-type tetrapyrrole lanthanide single-ion magnet (SIM) exhibits an overall enhanced magnetic performance including a high blocking temperature (TB) of 30 K and large effective spin-reversal energy barrier of Ueff = 939 K, rendering it the best sandwich-type tetrapyrrole lanthanide SIM reported thus far.Entities:
Year: 2017 PMID: 29111697 DOI: 10.1021/acs.inorgchem.7b02010
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165