Tohgha Urice, Deol Kirandeep K, Porter Ashlin G, Bartko Samuel G, Choi Jung Kyu, Leonard Brian M, Varga Krisztina, Kubelka Jan, Muller Gilles, Balaz Milan
Department of Chemistry, University of Wyoming , 1000 East University Avenue, Laramie, Wyoming 82071, United States .
ACS Nano. 2013 Dec 23;7(12):11094-102. doi: 10.1021/nn404832f. Epub 2013 Nov 13.
Chiral thiol capping ligands L- and D-cysteines induced modular chiroptical properties in achiral cadmium selenide quantum dots (CdSe QDs). Cys-CdSe prepared from achiral oleic acid capped CdSe by postsynthetic ligand exchange displayed size-dependent electronic circular dichroism (CD) and circularly polarized luminescence (CPL). Opposite CPL signals were measured for the CdSe QDs capped with D- and L-cysteine. The CD profile and CD anisotropy varied with size of CdSe nanocrystals with largest anisotropy observed for CdSe nanoparticles of 4.4 nm. Magic angle spinning solid state NMR (MAS ssNMR) experiments suggested bidentate interaction between cysteine and the surface of CdSe. Time Dependent Density Functional Theory (TDDFT) calculations verified that attachment of L- and D-cysteine to the surface of model (CdSe)13 nanoclusters induces measurable opposite CD signals for the exitonic band of the nanocluster. The origin of the induced chirality is consistent with the hybridization of highest occupied CdSe molecular orbitals with those of the chiral ligand.
手性硫醇封端配体L-和D-半胱氨酸在非手性硒化镉量子点(CdSe QDs)中诱导了模块化的手性光学性质。通过后合成配体交换由非手性油酸封端的CdSe制备的Cys-CdSe表现出尺寸依赖性的电子圆二色性(CD)和圆偏振发光(CPL)。对于用D-和L-半胱氨酸封端的CdSe量子点,测量到相反的CPL信号。CD谱和CD各向异性随CdSe纳米晶体的尺寸而变化,对于4.4 nm的CdSe纳米颗粒观察到最大的各向异性。魔角旋转固态核磁共振(MAS ssNMR)实验表明半胱氨酸与CdSe表面之间存在双齿相互作用。含时密度泛函理论(TDDFT)计算证实,L-和D-半胱氨酸附着到模型(CdSe)13纳米团簇表面会为纳米团簇的激子带诱导出可测量的相反CD信号。诱导手性的起源与最高占据的CdSe分子轨道与手性配体的分子轨道的杂化一致。