Zhang, Y., Han, T., Gu, S., Zhou, T., Zhao, C., Guo, Y., Feng, X., Tong, B., Bing, J., Shi, J., Zhi, J., & Dong, Y. (2014). Mechanochromic behavior of aryl-substituted buta-1,3-diene derivatives with aggregation enhanced emission. Chemistry - A European Journal, 20(29), 8856-8861. https://doi.org/10.1002/chem.201403132
Zhang, Yijia ; Han, Ting ; Gu, Shangzhi et al. / Mechanochromic behavior of aryl-substituted buta-1,3-diene derivatives with aggregation enhanced emission. In: Chemistry - A European Journal. 2014 ; Vol. 20, No. 29. pp. 8856-8861.
@article{d61f2f17ef994906abfb74a4f8d40078,
title = "Mechanochromic behavior of aryl-substituted buta-1,3-diene derivatives with aggregation enhanced emission",
abstract = "Three tetra-aryl substituted 1,3-butadiene derivatives with aggregation enhanced emission (AEE) and mechanochromic fluorescence behavior have been rationally designed and synthesized. The results suggest an effective design strategy for developing diverse materials with aggregation induced emission (AIE) and significant mechanochromic performance by employing D-π-A structures with large dipole moments. Mechanochromic luminescence: Three tetra-aryl substituted 1,3-butadiene derivatives with distinct electronic push and/or pull substituents have been prepared. All three derivatives show typical aggregation enhanced emission (AEE) features owing to the restriction of intramolecular rotations. The results demonstrate that chromophores with both large dipole moments and AEE characteristics are of benefit for mechanochromic applications with efficient solid-state emissions.",
keywords = "1,3-butadiene, aggregation enhanced emission, chromophores, fluorescence, mechanochromic luminescence",
author = "Yijia Zhang and Ting Han and Shangzhi Gu and Tianye Zhou and Chuanzhen Zhao and Yuexin Guo and Xiao Feng and Bin Tong and J. Bing and Jianbing Shi and Junge Zhi and Yuping Dong",
year = "2014",
month = jul,
day = "14",
doi = "10.1002/chem.201403132",
language = "English",
volume = "20",
pages = "8856--8861",
journal = "Chemistry - A European Journal",
issn = "0947-6539",
publisher = "Wiley-VCH Verlag",
number = "29",
}
Zhang, Y, Han, T, Gu, S, Zhou, T, Zhao, C, Guo, Y, Feng, X, Tong, B, Bing, J, Shi, J, Zhi, J & Dong, Y 2014, 'Mechanochromic behavior of aryl-substituted buta-1,3-diene derivatives with aggregation enhanced emission', Chemistry - A European Journal, vol. 20, no. 29, pp. 8856-8861. https://doi.org/10.1002/chem.201403132
Mechanochromic behavior of aryl-substituted buta-1,3-diene derivatives with aggregation enhanced emission. / Zhang, Yijia; Han, Ting; Gu, Shangzhi et al.
In:
Chemistry - A European Journal, Vol. 20, No. 29, 14.07.2014, p. 8856-8861.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Mechanochromic behavior of aryl-substituted buta-1,3-diene derivatives with aggregation enhanced emission
AU - Zhang, Yijia
AU - Han, Ting
AU - Gu, Shangzhi
AU - Zhou, Tianye
AU - Zhao, Chuanzhen
AU - Guo, Yuexin
AU - Feng, Xiao
AU - Tong, Bin
AU - Bing, J.
AU - Shi, Jianbing
AU - Zhi, Junge
AU - Dong, Yuping
PY - 2014/7/14
Y1 - 2014/7/14
N2 - Three tetra-aryl substituted 1,3-butadiene derivatives with aggregation enhanced emission (AEE) and mechanochromic fluorescence behavior have been rationally designed and synthesized. The results suggest an effective design strategy for developing diverse materials with aggregation induced emission (AIE) and significant mechanochromic performance by employing D-π-A structures with large dipole moments. Mechanochromic luminescence: Three tetra-aryl substituted 1,3-butadiene derivatives with distinct electronic push and/or pull substituents have been prepared. All three derivatives show typical aggregation enhanced emission (AEE) features owing to the restriction of intramolecular rotations. The results demonstrate that chromophores with both large dipole moments and AEE characteristics are of benefit for mechanochromic applications with efficient solid-state emissions.
AB - Three tetra-aryl substituted 1,3-butadiene derivatives with aggregation enhanced emission (AEE) and mechanochromic fluorescence behavior have been rationally designed and synthesized. The results suggest an effective design strategy for developing diverse materials with aggregation induced emission (AIE) and significant mechanochromic performance by employing D-π-A structures with large dipole moments. Mechanochromic luminescence: Three tetra-aryl substituted 1,3-butadiene derivatives with distinct electronic push and/or pull substituents have been prepared. All three derivatives show typical aggregation enhanced emission (AEE) features owing to the restriction of intramolecular rotations. The results demonstrate that chromophores with both large dipole moments and AEE characteristics are of benefit for mechanochromic applications with efficient solid-state emissions.
KW - 1,3-butadiene
KW - aggregation enhanced emission
KW - chromophores
KW - fluorescence
KW - mechanochromic luminescence
UR - http://www.scopus.com/inward/record.url?scp=84904040291&partnerID=8YFLogxK
U2 - 10.1002/chem.201403132
DO - 10.1002/chem.201403132
M3 - Article
AN - SCOPUS:84904040291
SN - 0947-6539
VL - 20
SP - 8856
EP - 8861
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 29
ER -
Zhang Y, Han T, Gu S, Zhou T, Zhao C, Guo Y et al. Mechanochromic behavior of aryl-substituted buta-1,3-diene derivatives with aggregation enhanced emission. Chemistry - A European Journal. 2014 Jul 14;20(29):8856-8861. doi: 10.1002/chem.201403132
