材料科学
共价键
密度泛函理论
光致发光
单层
共轭体系
光化学
动态光散射
酞菁
猝灭(荧光)
结合
荧光
吸收(声学)
化学工程
纳米技术
纳米颗粒
有机化学
化学
计算化学
聚合物
复合材料
光电子学
数学分析
物理
数学
工程类
量子力学
作者
Kazi M. Alam,Pawan Kumar,Sergey Gusarov,Alexander E. Kobryn,Aarat P. Kalra,Sheng Zeng,Ankur Goswami,Thomas Thundat,Karthik Shankar
标识
DOI:10.1021/acsami.0c07179
摘要
We report highly fluorescent cellulose nanocrystals (CNCs) formed by conjugating a carboxylated zinc phthalocyanine (ZnPc) to two different types of CNCs. The conjugated nanocrystals (henceforth called ZnPc@CNCs) were bright green in color and exhibited absorption and emission maxima at ∼690 and ∼715 nm, respectively. The esterification protocol employed to covalently bind carboxylated ZnPc to surface hydroxyl group rich CNCs was expected to result in a monolayer of ZnPc on the surface of the CNCs. However, dynamic light scattering (DLS) studies indicated a large increase in the hydrodynamic radius of CNCs following conjugation to ZnPc, which suggests the binding of multiple ZnPc molecular layers on the CNC surface. This binding could be through co-facial π-stacking of ZnPc, where ZnPc metallophthalocyanine rings are horizontal to the CNC surface. The other possible binding mode would give rise to conjugated systems where ZnPc metallophthalocyanine rings are oriented vertically on the CNC surface. Density functional theory based calculations showed stable geometry following the conjugation protocol that involved covalently attached ester bond formation. The conjugates demonstrated superior performance for potential sensing applications through higher photoluminescence quenching capabilities compared to pristine ZnPc.
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