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Synthesis of an antimony rhodamine analog

George Rajendra Kumar 1
George Rajendra Kumar
, 
Mengxi Yang 1
Mengxi Yang
, 
Benyu Zhou 1
Benyu Zhou
, 
Francois P Gabbai 1
Francois P Gabbai
1 Department of Chemistry, Texas A and M University, College Station, TX, USA
10.1016/j.mencom.2022.01.021
Published 2022-01-03
Communication , Volume 32, Issue 1, 66-67
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Kumar G. R. et al. Synthesis of an antimony rhodamine analog // Mendeleev Communications. 2022. Vol. 32. No. 1. pp. 66-67.
GOST all authors (up to 50) Copy
Kumar G. R., Yang M., Zhou B., Gabbai F. P. Synthesis of an antimony rhodamine analog // Mendeleev Communications. 2022. Vol. 32. No. 1. pp. 66-67.
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TY - JOUR
DO - 10.1016/j.mencom.2022.01.021
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.01.021
TI - Synthesis of an antimony rhodamine analog
T2 - Mendeleev Communications
AU - Kumar, George Rajendra
AU - Yang, Mengxi
AU - Zhou, Benyu
AU - Gabbai, Francois P
PY - 2022
DA - 2022/01/03
PB - Mendeleev Communications
SP - 66-67
IS - 1
VL - 32
ER -
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@article{2022_Kumar,
author = {George Rajendra Kumar and Mengxi Yang and Benyu Zhou and Francois P Gabbai},
title = {Synthesis of an antimony rhodamine analog},
journal = {Mendeleev Communications},
year = {2022},
volume = {32},
publisher = {Mendeleev Communications},
month = {Jan},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.01.021},
number = {1},
pages = {66--67},
doi = {10.1016/j.mencom.2022.01.021}
}
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Kumar, George Rajendra, et al. “Synthesis of an antimony rhodamine analog.” Mendeleev Communications, vol. 32, no. 1, Jan. 2022, pp. 66-67. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.01.021.

Keywords

crystal structure
fluorescence
organoantimony compounds
rhodamine
synthesis

Abstract

We describe the synthesis, structure and characterization of an antimony-rhodamine derivative with a phenyl-antimony moiety installed at the 10' position of the central ring. This compound is a red fluorophore (λem = 655 nm) with a quantum yield of 12% in acetonitrile.

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