摘要
以2-苯胺基-4,6-二叔丁基苯酚(H2L) 和 FeCl2·4H2O 为原料制备了一对手性半醌 Fe(III) 络合物Λ-mer-[Fe(LISQ)3]和Δ-mer-[Fe(LISQ)3] (LISQ: 2-苯亚胺基-4,6-二叔丁基苯酚, mer : 经式构型), 通过单晶 X 射线衍射分析结合单晶压制片膜的固体圆二色(CD)光谱确定了该络合物的绝对构型, 在此基础上建立了此类半醌络合物[M(LISQ)3] (M=Cr, Fe, Co)的惟手性金属中心绝对构型与固体 CD 光谱之间的关联. 此外, 还对 10 份合成的[Fe(LISQ)3]的大宗产物粉末与单晶的固体 CD 谱进行了比对分析, 以及对 1 份合成产物进行 10 次重结晶的固体CD 光谱表征. 研究表明该化合物在结晶过程中发生了镜面对称性破缺 (MSB), 对映体过量 (ee) 值在15%-100%之间.
A pair of chiral o-iminobenzosemiquinonato Fe（Ⅲ） complexes, A-mer-[Fe（LlSQ）3] and Zl-mer- [Fe（LlSQ）3] （LlSQ： 2-phenylimino-4,6-di-tert-butylphenol, mer： meridian configuration）, were synthesized from 2-anilino-4,6-di-tert-butylphenol （H2L） and FeCI2· 4H20. Their absolute configurations were determined by single crystal X-ray diffraction （XRD） and solid-state circular dichroism （CD） spectra （the same single crystal for XRD was dispersed in KCI）. Correlations between the absolute configurations of the chiral-at- metal o-iminobenzosemiquinonato M（III） complexes [M（LlSQ）3] （M=Cr, Fe, Co） and their solid-state CD spectra were also established. Comparison between solid-state CD spectra of the bulk samples from 10 different syntheses and their single crystals were thoroughly analyzed. The solid-state CD spectra of the powdered samples from 10 different crystallizations of one product were characterized. These studies indicated that mirror symmetry breaking （MSB） occurred during the crystallization process of the Fe（lll） complexes and their enantiomeric excess （ee） values were between 15% and 100%.
出处
《物理化学学报》
SCIE
CAS
CSCD
北大核心
2013年第6期1183-1191,共9页
Acta Physico-Chimica Sinica
基金
国家自然科学基金(21273175, 20973136)资助项目~~
关键词
半醌Fe(Ⅲ)络合物
镜面对称性破缺
绝对构型
固体CD光谱
单晶X射线衍射
Semiquinone Fe（Ⅲ） complexes
Mirror symmetry breaking
Absolute configuration
Solid-state CD spectroscopy
Single crystal X-ray diffraction
