TY - JOUR
T1 - Zwitterionic Cyanine-Cyanine Salt
T2 - Structure and Optical Properties
AU - Li, Zhong'An
AU - Zhao, Peng
AU - Tofighi, Salimeh
AU - Sharma, Rajesh
AU - Ensley, Trenton R.
AU - Jang, Sei-Hum
AU - Hagan, David J.
AU - Van Stryland, Eric W.
AU - Jen, Alex K.-Y.
PY - 2016/7/21
Y1 - 2016/7/21
N2 - Cyanines with long conjugation length such as heptamethines are well known to have strong intramolecular and/or intermolecular interactions (i.e., ion paring and aggregation), which can affect their structures (i.e., symmetry breaking) and optical properties remarkably. In this paper, we report a covalently linked complementary cyanine complex of cationic and anionic heptamethines forming a highly polarizable zwitterionic cyanine-cyanine salt. The effect of the modification was studied in detail on both its electronic structure and its optical properties. This novel zwitterionic salt was found to exhibit a decreased ion-pairing-induced charge localization but with an increased electronic coupling between the excited states of the cyanine cation and the anion, resulting in unusual optical properties compared to closely related noncovalent complementary cyanine salts. The dual-arm Z-scan technique was used to study their third-order NLO properties, suggesting the electronic coupling in such preorganized zwitterionic system has a weak impact on NLO properties, and both cyanines contribute to the large third-order molecular polarizabilities exceeding 4 × 10-32 esu for potential all-optical photonic applications.
AB - Cyanines with long conjugation length such as heptamethines are well known to have strong intramolecular and/or intermolecular interactions (i.e., ion paring and aggregation), which can affect their structures (i.e., symmetry breaking) and optical properties remarkably. In this paper, we report a covalently linked complementary cyanine complex of cationic and anionic heptamethines forming a highly polarizable zwitterionic cyanine-cyanine salt. The effect of the modification was studied in detail on both its electronic structure and its optical properties. This novel zwitterionic salt was found to exhibit a decreased ion-pairing-induced charge localization but with an increased electronic coupling between the excited states of the cyanine cation and the anion, resulting in unusual optical properties compared to closely related noncovalent complementary cyanine salts. The dual-arm Z-scan technique was used to study their third-order NLO properties, suggesting the electronic coupling in such preorganized zwitterionic system has a weak impact on NLO properties, and both cyanines contribute to the large third-order molecular polarizabilities exceeding 4 × 10-32 esu for potential all-optical photonic applications.
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U2 - 10.1021/acs.jpcc.6b03037
DO - 10.1021/acs.jpcc.6b03037
M3 - RGC 21 - Publication in refereed journal
SN - 1932-7447
VL - 120
SP - 15378
EP - 15384
JO - The Journal of Physical Chemistry C
JF - The Journal of Physical Chemistry C
IS - 28
ER -