Tuning of hyperpolarizability, and one- and two-photon absorption of donor–acceptor and donor–acceptor–acceptor-type intramolecular charge transfer-based sensors. Issue 31 (29th July 2019)
- Record Type:
- Journal Article
- Title:
- Tuning of hyperpolarizability, and one- and two-photon absorption of donor–acceptor and donor–acceptor–acceptor-type intramolecular charge transfer-based sensors. Issue 31 (29th July 2019)
- Main Title:
- Tuning of hyperpolarizability, and one- and two-photon absorption of donor–acceptor and donor–acceptor–acceptor-type intramolecular charge transfer-based sensors
- Authors:
- Samanta, Pralok K.
Alam, Md. Mehboob
Misra, Ramprasad
Pati, Swapan K. - Abstract:
- Abstract : Effect of solvent as well as arrangement of donor–acceptor groups on the linear and non-linear optical (NLO) response properties of two intramolecular charge-transfer (ICT)-based fluorescent sensors are studied. Abstract : The present work aims to study the effect of solvent as well as arrangement of donor–acceptor groups on linear and non-linear optical (NLO) response properties of two experimentally studied intramolecular charge-transfer (ICT)-based fluorescent sensors. One of them (molecule1 ) is a donor–acceptor (D–A) system with hemicyanine and dimethylanilino as electron withdrawing and donating groups, respectively, while the other one (molecule3 ) is molecule1 fused with a boron-dipyrromethene (BODIPY) moiety. BODIPY acts as the electron acceptor group of molecule2 that as well consists of dimethylanilino as the electron donor. Density functional theory (DFT) as well as time-dependent DFT has been employed to optimize the geometry of the molecules, followed by computation of dipole moment ( μ ), static first hyperpolarizability ( β total ), and one- and two-photon absorption (TPA) strengths. The results reveal that dipole moment as well as total static first hyperpolarizability ( β total ) of the studied molecules is dominated by the respective components in the direction of charge transfer. The ratio of vector component of first hyperpolarizability ( β vec ) to β total also supports the unidirectional charge transfer in the studied systems. In molecule3,Abstract : Effect of solvent as well as arrangement of donor–acceptor groups on the linear and non-linear optical (NLO) response properties of two intramolecular charge-transfer (ICT)-based fluorescent sensors are studied. Abstract : The present work aims to study the effect of solvent as well as arrangement of donor–acceptor groups on linear and non-linear optical (NLO) response properties of two experimentally studied intramolecular charge-transfer (ICT)-based fluorescent sensors. One of them (molecule1 ) is a donor–acceptor (D–A) system with hemicyanine and dimethylanilino as electron withdrawing and donating groups, respectively, while the other one (molecule3 ) is molecule1 fused with a boron-dipyrromethene (BODIPY) moiety. BODIPY acts as the electron acceptor group of molecule2 that as well consists of dimethylanilino as the electron donor. Density functional theory (DFT) as well as time-dependent DFT has been employed to optimize the geometry of the molecules, followed by computation of dipole moment ( μ ), static first hyperpolarizability ( β total ), and one- and two-photon absorption (TPA) strengths. The results reveal that dipole moment as well as total static first hyperpolarizability ( β total ) of the studied molecules is dominated by the respective components in the direction of charge transfer. The ratio of vector component of first hyperpolarizability ( β vec ) to β total also supports the unidirectional charge transfer in the studied systems. In molecule3, which is a donor–acceptor–acceptor (D–A–A)-type system, the BODIPY moiety is found to play a major role in controlling the NLO response over the other acceptor group. Solvents are also found to play an important role in controlling the linear as well as NLO response of the studied systems. A significant increase in the first hyperpolarizability as well as TPA cross-section of the studied molecules is predicted due to an increase in the dielectric constant of the medium. The results presented are expected to provide a clue in tuning the NLO response of many ICT-based chromophores, especially those with D–A–A arrangements. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 21:Issue 31(2019)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 21:Issue 31(2019)
- Issue Display:
- Volume 21, Issue 31 (2019)
- Year:
- 2019
- Volume:
- 21
- Issue:
- 31
- Issue Sort Value:
- 2019-0021-0031-0000
- Page Start:
- 17343
- Page End:
- 17355
- Publication Date:
- 2019-07-29
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9cp03772a ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11349.xml