Issue 48, 2015

Morphology-controlled assembly and enhanced emission of fluorescence in organic nanospheres and microrods based on 1,2-diphenyl-4-(4-dibenzothienyl)phenyl-1,3-cyclopentadiene

Abstract

Fluorescent organic nanospheres, pod-like connecting spheres and microrods based on 1,2-diphenyl-4-(4-dibenzothienyl)phenyl-1,3-cyclopentadiene (DPCP) have been prepared via controlling the solvent composition. The influence of concentration, surfactants and solvents on the morphologies of products was examined. The formation of particles with different morphologies could be attributed to the solubility-controlled crystalline nucleation. Single crystal X-ray analysis reveals that the molecule of DPCP has a non-coplanar geometry, and two molecules are packed to form a dimer as an X-aggregate. Further, one-dimensional chains of DPCP additionally avoided the maximum face-to-face stacking. The solution of DPCP in methanol has weaker emission with a peak at 455 nm, however, the nanospheres, pod-like connecting spheres and microrods exhibited remarkably enhanced fluorescence emission with peaks at 447, 448 and 468 nm, respectively. Additionally, fluorescence change behavior was further verified by DFT calculation and time-resolved emission decay measurements.

Graphical abstract: Morphology-controlled assembly and enhanced emission of fluorescence in organic nanospheres and microrods based on 1,2-diphenyl-4-(4-dibenzothienyl)phenyl-1,3-cyclopentadiene

Supplementary files

Article information

Article type
Paper
Submitted
18 Sep 2015
Accepted
06 Nov 2015
First published
09 Nov 2015

CrystEngComm, 2015,17, 9311-9317

Author version available

Morphology-controlled assembly and enhanced emission of fluorescence in organic nanospheres and microrods based on 1,2-diphenyl-4-(4-dibenzothienyl)phenyl-1,3-cyclopentadiene

J. Ye, X. Huang, Y. Gao, X. Wang, T. Zheng, Y. Lin, X. Liu and G. Ning, CrystEngComm, 2015, 17, 9311 DOI: 10.1039/C5CE01849H

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