Theoretical Understanding of Photoluminescence and Singlet Oxygen Quantum Yields in a Few Halogenated Fluorescein Dyes

被引:0
作者
Tedy, Annette Mariya [1 ]
Manna, Arun K. [1 ]
机构
[1] Indian Inst Technol Tirupati, Dept Chem, Tirupati 517619, India
关键词
Halogenated fluorescein dyes; Photoluminescence; Singlet oxygen quantum yield; Range-Separated Hybrid; INTERSYSTEM CROSSING RATES; EXCITED-STATES; XANTHENE DYES; ABSORPTION; APPROXIMATION; FUNCTIONALS; TRANSITIONS; COUPLINGS; LIFETIME;
D O I
10.1002/asia.202401065
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Visible-light absorbing metal-free organic dyes are of increasing demand for various optoelectronic applications because of their great structure-function tunability through chemical means. Several dyes also show huge potential in triplet photosensitization, generating reactive singlet oxygen. Understanding the structure-property relationships of many well-known fluorescein dyes is of paramount importance in designing next-generation energy efficient dyes, which is currently limited. For example, the role of heavy atoms in the excited-state deactivations is not fully understood for these dyes. Herein, 9 halogenated (Cl, Br, I) fluorescein dyes with varied halogen concentrations and positions are studied using time-dependent range-separated hybrid combined with polarizable continuum model with water dielectric for accounting of polarization and screening effects. Excited state energies of these dyes and their deactivations via radiative and non-radiative pathways are well described using 0-0 corrected excitation energies. Calculated results are in reasonable agreement with the available experimental data. However, no systematic correlation is found between the heavy-atom effect and calculated intersystem crossing/fluorescence rates. Not surprisingly, heavy-atom effect is found to be more pronounced in iodinated dyes compared to their brominated analogues. Halogen position also plays a critical role in determining the excited-state deactivation rates. All dyes show similar fluorescence rates of similar to 10(8) s(-1) . Whereas, the intersystem crossing rates are much smaller and vary from similar to 10(2) to 10(4) s(-1) . Nevertheless, lower fluorescence quantum yields for some dyes are attributed to the large internal conversion. Microscopic understanding on the excited-state properties of several halogenated fluorescein dyes reported here will aid in developing advanced fluorescein dye based energy efficient photosensitizers and also emitters.
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页数:11
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共 60 条
[1]   Understanding remarkably high triplet quantum yield in thione analogs of perylenediimide: A detailed theoretical study [J].
Ahmed, Raka ;
Manna, Arun K. .
JOURNAL OF CHEMICAL PHYSICS, 2023, 158 (21)
[2]  
Ahmed R, 2022, J PHYS CHEM A, V126, P6594, DOI 10.1021/acs.jpca.2c03455
[3]   Tailoring intersystem crossing of perylenediimide through chalcogen-substitution at bay-position: A theoretical perspective [J].
Ahmed, Raka ;
Manna, Arun K. .
JOURNAL OF CHEMICAL PHYSICS, 2022, 157 (21)
[4]   Design of BODIPY dyes as triplet photosensitizers: electronic properties tailored for solar energy conversion, photoredox catalysis and photodynamic therapy [J].
Bassan, Elena ;
Gualandi, Andrea ;
Cozzi, Pier Giorgio ;
Ceroni, Paola .
CHEMICAL SCIENCE, 2021, 12 (19) :6607-6628
[5]   Intersystem Crossing in Tetrapyrrolic Macrocycles. A First-Principles Analysis [J].
Bhandari, Srijana ;
Sarkar, Sunandan ;
Schubert, Alexander ;
Yamada, Atsushi ;
Payne, Jameson ;
Ptaszek, Marcin ;
Geva, Eitan ;
Dunietz, Barry D. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2021, 125 (24) :13493-13500
[6]   Electron transfer - From isolated molecules to biomolecules [J].
Bixon, M ;
Jortner, J .
ELECTRON TRANSFER-FROM ISOLATED MOLECULES TO BIOMOLECULES, PT 1, 1999, 106 :35-202
[7]   Charge-transfer and energy-transfer processes in π-conjugated oligomers and polymers:: A molecular picture [J].
Brédas, JL ;
Beljonne, D ;
Coropceanu, V ;
Cornil, J .
CHEMICAL REVIEWS, 2004, 104 (11) :4971-5003
[8]   Long-range corrected hybrid density functionals with damped atom-atom dispersion corrections [J].
Chai, Jeng-Da ;
Head-Gordon, Martin .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2008, 10 (44) :6615-6620
[9]   Troubleshooting time-dependent density-functional theory for photochemical applications: Oxirane [J].
Cordova, Felipe ;
Doriol, L. Joubert ;
Ipatov, Andrei ;
Casidaa, Mark E. ;
Filippi, Claudia ;
Vela, Alberto .
JOURNAL OF CHEMICAL PHYSICS, 2007, 127 (16)
[10]   PHOTOPHYSICAL STUDIES ON POLYHALOGENATED XANTHENE DYES [J].
ELCOV, AW ;
SMIRNOVA, NP ;
PONYAEV, AI ;
MARTINOVA, WP ;
SCHUTZ, R ;
HARTMANN, H .
JOURNAL OF LUMINESCENCE, 1990, 47 (03) :99-105