Rational design and investigation of nonlinear optical response properties of pyrrolopyrrole aza-BODIPY-based novel push-pull chromophores

被引:1
|
作者
Kothoori, Naga Pranava Sree [1 ]
Sivasakthi, Pandiyan [1 ,3 ]
Baithy, Mallesham [1 ]
Misra, Ramprasad [2 ]
Samanta, Pralok K. [1 ,3 ]
机构
[1] Gandhi Inst Technol & Management GITAM, Sch Sci, Dept Chem, Hyderabad 502329, India
[2] Humboldt Univ, Inst Biol, Expt Biophys, D-10115 Berlin, Germany
[3] Birla Inst Technol & Sci Pilani BITS Pilani, Dept Chem, Hyderabad Campus, Hyderabad 500078, India
关键词
2-PHOTON ABSORPTION; DONOR; DERIVATIVES; PARAMETER; POLYENES; RANGE; DYES; DFT;
D O I
10.1039/d4ra02861a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Intramolecular charge transfer (ICT)-based chromophores are highly sought after for designing near-infrared (NIR) absorbing and emitting dyes as well as for designing materials for nonlinear optical (NLO) applications. The properties of these 'push-pull' molecules can easily be modified by varying the electronic donor (D) and acceptor (A) groups as well as the pi-conjugation linker. This study presents a methodical approach and employs quantum chemical analysis to explore the relationship between the structural features, electro-optical properties, and the NLO characteristics of molecules with D-pi-A framework. The one- and two-photon absorption (2PA), linear polarizability (alpha), and first hyperpolarizability (beta) of some novel chromophores, consisting of a dimeric aza-Boron Dipyrromethene (aza-BODIPY) analogue, called, pyrrolopyrrole aza-BODIPY (PPAB), serving as the acceptor, have been investigated. The electronic donors used in this study are triphenylamine (TPA) and diphenylamine (DPA), and they are conjugated to the acceptor via thienyl or phenylene pi-linkers. Additionally, the Hyper-Rayleigh Scattering (beta HRS), which enables direct estimation of the second-order NLO properties, is calculated for the studied chromophores with 1064 nm excitation in acetonitrile. The beta value shows a significant increase with increasing solvent polarity, indicating that the ICT plays a crucial role in shaping the NLO response of the studied molecules. The enhancement of the 2PA cross-section of the investigated molecules can also be achieved by modulating the combinations of donors and linkers. The results of our study indicate that the novel D-pi-A molecules designed in this work demonstrate considerably higher hyperpolarizability values than the standard p-nitroaniline, making them promising candidates for future NLO applications. Intramolecular charge transfer plays crucial role in shaping linear and nonlinear optical response properties of novel pyrrolopyrrole aza-BODIPY-based push-pull chromophores.
引用
收藏
页码:15560 / 15570
页数:11
相关论文
共 50 条
  • [31] Multipodal arrangement of push-pull chromophores: a fundamental parameter affecting their electronic and optical properties
    Klikar, M.
    Kityk, I. V.
    Kulwas, D.
    Mikysek, T.
    Pytela, O.
    Bures, F.
    NEW JOURNAL OF CHEMISTRY, 2017, 41 (04) : 1459 - 1472
  • [32] Synthesis and Photophysical Properties of a Series of Pyrazine-Based Push-Pull Chromophores
    Hoffert, Kellyn
    Durand, Raphael J.
    Gauthier, Sebastien
    Robin-le Guen, Francoise
    Achelle, Sylvain
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2017, 2017 (03) : 523 - 529
  • [33] Quadratic nonlinear optical response of composite polymer materials based on push-pull quinoxaline chromophores with various groups in the aniline donor moiety
    Kalinin, Alexey A.
    Islamova, Liliya N.
    Sharipova, Sirina M.
    Fazleeva, Guzel M.
    Gaysin, Adel I.
    Shmelev, Artemiy G.
    Simanchuk, Andrey E.
    Turgeneva, Snezhana A.
    Sharipova, Anastasiya V.
    Mukhtarov, Anvar S.
    Vakhonina, Tatyana A.
    Fominykh, Olga D.
    Mikerin, Sergey L.
    Balakina, Marina Yu.
    NEW JOURNAL OF CHEMISTRY, 2023, 47 (05) : 2296 - 2306
  • [34] New push-pull ladder-type chromophores with large hyperpolarizability for nonlinear optical application
    Sun, Hejing
    STRUCTURAL CHEMISTRY, 2025, 36 (01) : 39 - 48
  • [35] Nonlinear optical properties of push-pull stilbenes based on a strong carbocation acceptor moiety
    Paci, B
    Schmidt, C
    Fiorini, C
    Nunzi, JM
    Arbez-Gindre, C
    Screttas, CG
    JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (16): : 7486 - 7492
  • [36] Nonlinear optical properties of push-pull polyenes for electro-optics
    Stahelin, M
    Zysset, B
    Ahlheim, M
    Marder, SR
    Bedworth, PV
    Runser, C
    Barzoukas, M
    Fort, A
    JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS, 1996, 13 (11) : 2401 - 2407
  • [37] Small isomeric push-pull chromophores based on thienothiophenes with tunable optical (non)linearities
    Podlesny, Jan
    Pytela, Oldrich
    Klikar, Milan
    Jelinkova, Veronika
    Kityk, Iwan V.
    Ozga, Katarzyna
    Jedryka, Jaroslaw
    Rudysh, Myron
    Bures, Filip
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2019, 17 (14) : 3623 - 3634
  • [38] The effectiveness of essential-state models in the description of optical properties of branched push-pull chromophores
    Sissa, Cristina
    Parthasarathy, Venkatakrishnan
    Drouin-Kucma, Delphine
    Werts, Martinus H. V.
    Blanchard-Desce, Mireille
    Terenziani, Francesca
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2010, 12 (37) : 11715 - 11727
  • [39] Novel thiophene-containing push-pull chromophores that include carbazole and triphenylamine moieties: study of optical and electrochemical properties
    Bakiev, Artur N.
    Selivanova, Darya G.
    Lunegov, Igor V.
    Vasyanin, Aleksandr N.
    Maiorova, Olga A.
    Gorbunov, Aleksei A.
    Shklyaeva, Elena V.
    Abashev, Georgii G.
    CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2016, 52 (06) : 379 - 387
  • [40] Novel thiophene-containing push-pull chromophores that include carbazole and triphenylamine moieties: study of optical and electrochemical properties
    Artur N. Bakiev
    Darya G. Selivanova
    Igor V. Lunegov
    Aleksandr N. Vasyanin
    Olga A. Maiorova
    Aleksei A. Gorbunov
    Elena V. Shklyaeva
    Georgii G. Abashev
    Chemistry of Heterocyclic Compounds, 2016, 52 : 379 - 387