TY - JOUR
T1 - Properties of polymorphism and acid response of pyrrolopyrrole-based derivative with aggregation-induced emission behavior
AU - Peng, Zhe
AU - Ji, Yingchun
AU - Wang, Zhi
AU - Tong, Bin
AU - Shi, Jianbing
AU - Dong, Yuping
N1 - Publisher Copyright:
© 2016 Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences.
PY - 2016/11/15
Y1 - 2016/11/15
N2 - A new A-D-A type pyrrolopyrrole-based derivative 4′,4″-(2,5-diphenyl-pyrrolo[3,2-b]pyrrole-1,4-diyl)bis ([1,1'-biphenyl]-4-carbonitrile) (DPPDC) was synthesized via Suzuki coupling reaction between 1,4-bis(4-bromophenyl)-2,5-diphenyl-1,4-dihydropyrrolo[3,2-b]pyrrole and 4-cyanophenylboronic acid. The fluorescent emission intensities of DPPDC in pure THF solution and lower fraction of water (φH2O≤60%) mixtures were weak at around 550 nm. When φH2O was 99% in THF/H2O mixtures, the emission was enhanced and blue-shifted at around 505 nm. The maximal fluorescent emission intensity of DPPDC was 11 times higher than that of in pure THF solution, indicating DPPDC exhibiting AIE property. It was also found that four different kinds of crystal structures of DPPDC was cultivated from CHCl2-Hexane, CHCl3-Hexane and CHCl3/Acetone-Hexane systems via solvent slow diffusion method. Four crystals respec-tively emitted blue, azure, green and turquoise at 467, 483, 496 and 493 nm, which manifested the polymorphism-dependent fluorescent emission property of DPPDC. Additionally, trifluoroacetic acid (TFA) could make the emitting color change from yellow to orange-red with as-prepared paper containing DPPDC due to the acid-base interaction. The obvious emitting color change of DPPDC can be used as a visual sensor to detect acid gas.
AB - A new A-D-A type pyrrolopyrrole-based derivative 4′,4″-(2,5-diphenyl-pyrrolo[3,2-b]pyrrole-1,4-diyl)bis ([1,1'-biphenyl]-4-carbonitrile) (DPPDC) was synthesized via Suzuki coupling reaction between 1,4-bis(4-bromophenyl)-2,5-diphenyl-1,4-dihydropyrrolo[3,2-b]pyrrole and 4-cyanophenylboronic acid. The fluorescent emission intensities of DPPDC in pure THF solution and lower fraction of water (φH2O≤60%) mixtures were weak at around 550 nm. When φH2O was 99% in THF/H2O mixtures, the emission was enhanced and blue-shifted at around 505 nm. The maximal fluorescent emission intensity of DPPDC was 11 times higher than that of in pure THF solution, indicating DPPDC exhibiting AIE property. It was also found that four different kinds of crystal structures of DPPDC was cultivated from CHCl2-Hexane, CHCl3-Hexane and CHCl3/Acetone-Hexane systems via solvent slow diffusion method. Four crystals respec-tively emitted blue, azure, green and turquoise at 467, 483, 496 and 493 nm, which manifested the polymorphism-dependent fluorescent emission property of DPPDC. Additionally, trifluoroacetic acid (TFA) could make the emitting color change from yellow to orange-red with as-prepared paper containing DPPDC due to the acid-base interaction. The obvious emitting color change of DPPDC can be used as a visual sensor to detect acid gas.
KW - Acid response
KW - Aggregation-induced emission
KW - Polymorphism
KW - Pyrrolopyrrole
UR - http://www.scopus.com/inward/record.url?scp=85006386889&partnerID=8YFLogxK
U2 - 10.6023/A16080406
DO - 10.6023/A16080406
M3 - Article
AN - SCOPUS:85006386889
SN - 0567-7351
VL - 74
SP - 942
EP - 948
JO - Acta Chimica Sinica
JF - Acta Chimica Sinica
IS - 11
ER -