Tunable photophysical properties of thiophene based chromophores: a conjoined experimental and theoretical investigation

In this paper we report the synthesis and photophysical properties of six novel thiophene derivatives (ThD) with D-π-A structure. The subject of this work is three nitrophenyls ( 1 ) BT-Th-NO 2 and three benzonitriles ( 2 ) BT-Th-CN, substituted at different positions of the aromatic ring (( a ) ort...

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Published inNew journal of chemistry Vol. 43; no. 17; pp. 6728 - 6736
Main Authors Popczyk, Anna, Cheret, Yohan, Grabarz, Anna, Hanczyc, Piotr, Fita, Piotr, El-Ghayoury, Abdelkrim, Sznitko, Lech, Mysliwiec, Jaroslaw, Sahraoui, Bouchta
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 22.04.2019
Royal Society of Chemistry
Royal Society of Chemistry [1987-....]
Subjects
Aromatic compounds
Carbon 13
Charge transfer
Chemical Sciences
Chemical synthesis
Chemistry
Chemistry, Multidisciplinary
Chromophores
Emission spectra
Fluorescence
Mass spectrometry
Mathematical analysis
Nitrogen dioxide
NMR
Nuclear magnetic resonance
Optical properties
Organic chemistry
Photoluminescence
Physical Sciences
Quantum chemistry
Science & Technology
STILBENE
2-PHOTON ABSORPTION
NONLINEAR-OPTICAL PROPERTIES
CONTINUUM
BIREFRINGENCE
DERIVATIVES
EFFICIENT
INTRAMOLECULAR CHARGE-TRANSFER
AZO-DYE
MOLECULES
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Abstract In this paper we report the synthesis and photophysical properties of six novel thiophene derivatives (ThD) with D-π-A structure. The subject of this work is three nitrophenyls ( 1 ) BT-Th-NO 2 and three benzonitriles ( 2 ) BT-Th-CN, substituted at different positions of the aromatic ring (( a ) ortho -, ( b ) meta - or ( c ) para -). Dyes were obtained using a simple three-step synthesis and their chemical structures were confirmed by 1 H and 13 C NMR, IR and high resolution mass spectrometry. The influence of positional isomerism on the optical properties has been explored experimentally and theoretically. The photophysical properties were investigated using steady-state and time-resolved spectroscopy and the obtained results were supported by quantum-chemical calculations. TD-DFT calculations indicated that the charge-transfer strength can be correlated with the observed optical properties. In addition, the influence of the acceptor position on the photoluminescence spectra, fluorescence quantum yields and emission lifetimes was specified. We show that the ThD optical properties can be tuned in a wide spectral range by a change made in only a single step of the synthesis reaction. Synthesis and theoretical investigation of six donor-acceptor thiophene based derivatives with tunable photophysical properties.
AbstractList In this paper we report the synthesis and photophysical properties of six novel thiophene derivatives (ThD) with D–π–A structure. The subject of this work is three nitrophenyls (1) BT-Th-NO2 and three benzonitriles (2) BT-Th-CN, substituted at different positions of the aromatic ring ((a) ortho-, (b) meta- or (c) para-). Dyes were obtained using a simple three-step synthesis and their chemical structures were confirmed by 1H and 13C NMR, IR and high resolution mass spectrometry. The influence of positional isomerism on the optical properties has been explored experimentally and theoretically. The photophysical properties were investigated using steady-state and time-resolved spectroscopy and the obtained results were supported by quantum-chemical calculations. TD-DFT calculations indicated that the charge-transfer strength can be correlated with the observed optical properties. In addition, the influence of the acceptor position on the photoluminescence spectra, fluorescence quantum yields and emission lifetimes was specified. We show that the ThD optical properties can be tuned in a wide spectral range by a change made in only a single step of the synthesis reaction.
In this paper we report the synthesis and photophysical properties of six novel thiophene derivatives (ThD) with D--A structure. The subject of this work is three nitrophenyls (1) BT-Th-NO2 and three benzonitriles (2) BT-Th-CN, substituted at different positions of the aromatic ring ((a) ortho-, (b) meta- or (c) para-). Dyes were obtained using a simple three-step synthesis and their chemical structures were confirmed by H-1 and C-13 NMR, IR and high resolution mass spectrometry. The influence of positional isomerism on the optical properties has been explored experimentally and theoretically. The photophysical properties were investigated using steady-state and time-resolved spectroscopy and the obtained results were supported by quantum-chemical calculations. TD-DFT calculations indicated that the charge-transfer strength can be correlated with the observed optical properties. In addition, the influence of the acceptor position on the photoluminescence spectra, fluorescence quantum yields and emission lifetimes was specified. We show that the ThD optical properties can be tuned in a wide spectral range by a change made in only a single step of the synthesis reaction.
In this paper we report the synthesis and photophysical properties of six novel thiophene derivatives (ThD) with D–π–A structure. The subject of this work is three nitrophenyls ( 1 ) BT-Th-NO 2 and three benzonitriles ( 2 ) BT-Th-CN, substituted at different positions of the aromatic ring (( a ) ortho -, ( b ) meta - or ( c ) para -). Dyes were obtained using a simple three-step synthesis and their chemical structures were confirmed by 1 H and 13 C NMR, IR and high resolution mass spectrometry. The influence of positional isomerism on the optical properties has been explored experimentally and theoretically. The photophysical properties were investigated using steady-state and time-resolved spectroscopy and the obtained results were supported by quantum-chemical calculations. TD-DFT calculations indicated that the charge-transfer strength can be correlated with the observed optical properties. In addition, the influence of the acceptor position on the photoluminescence spectra, fluorescence quantum yields and emission lifetimes was specified. We show that the ThD optical properties can be tuned in a wide spectral range by a change made in only a single step of the synthesis reaction.
In this paper we report the synthesis and photophysical properties of six novel thiophene derivatives (ThD) with D-π-A structure. The subject of this work is three nitrophenyls ( 1 ) BT-Th-NO 2 and three benzonitriles ( 2 ) BT-Th-CN, substituted at different positions of the aromatic ring (( a ) ortho -, ( b ) meta - or ( c ) para -). Dyes were obtained using a simple three-step synthesis and their chemical structures were confirmed by 1 H and 13 C NMR, IR and high resolution mass spectrometry. The influence of positional isomerism on the optical properties has been explored experimentally and theoretically. The photophysical properties were investigated using steady-state and time-resolved spectroscopy and the obtained results were supported by quantum-chemical calculations. TD-DFT calculations indicated that the charge-transfer strength can be correlated with the observed optical properties. In addition, the influence of the acceptor position on the photoluminescence spectra, fluorescence quantum yields and emission lifetimes was specified. We show that the ThD optical properties can be tuned in a wide spectral range by a change made in only a single step of the synthesis reaction. Synthesis and theoretical investigation of six donor-acceptor thiophene based derivatives with tunable photophysical properties.
Author Sznitko, Lech
Sahraoui, Bouchta
Fita, Piotr
El-Ghayoury, Abdelkrim
Popczyk, Anna
Hanczyc, Piotr
Mysliwiec, Jaroslaw
Grabarz, Anna
Cheret, Yohan
AuthorAffiliation Wroclaw University of Science and Technology
Faculty of Physics
University of Warsaw
CNRS
Laboratoire MOLTECH-Anjou
Faculty of Chemistry
Institute of Experimental Physics
UMR 6200
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Cites_doi 10.1016/j.optmat.2011.02.034
10.1063/1.434888
10.1016/j.jfluchem.2003.10.002
10.1002/adfm.201203209
10.1007/978-94-011-3370-8
10.1021/acsomega.8b01258
10.1021/acs.chemrev.6b00127
10.1063/1.2183309
10.1039/C5RA05912G
10.1039/C4RA11264D
10.1021/j100179a026
10.1039/c3sc22265a
10.1016/j.dyepig.2016.11.030
10.1039/c2cp40261k
10.1039/C7CS00162B
10.1016/j.dyepig.2017.06.012
10.1021/jp055449z
10.1038/nchem.2085
10.1021/cr9904009
10.1002/anie.200805257
10.1039/C7CP02249B
10.1021/acs.jpcc.6b03915
10.1021/ja960136q
10.1016/j.cap.2008.04.010
10.1039/C7TC05245F
10.1002/adma.19970090207
10.1002/anie.201310438
10.1021/cr980078m
10.1016/j.dyepig.2018.02.025
10.1021/ct200308m
10.1002/ejoc.200500372
10.1002/adma.200800604
10.1002/adma.201305999
10.1364/OL.22.001843
10.1002/adma.201470263
10.1038/451652a
10.1364/JOSAB.6.001339
10.1021/jp054250j
10.1002/anie.199500211
10.1021/acs.jctc.5b00538
10.1021/ma0493980
10.1038/srep40141
10.1021/acs.joc.5b02691
10.1021/cr040084k
10.1021/j100373a007
10.1002/adma.201100984
10.1039/C6RA26781E
10.1016/S0301-0104(99)00073-7
10.1016/0301-0104(81)85090-2
10.1002/adfm.200701150
10.1021/acs.jpcc.6b04849
10.1364/OL.24.001349
10.1021/jp0508913
10.1021/jp076447c
10.1002/wcms.1260
10.1039/c7cp02249b
10.1038/NCHEM.2085
10.1039/c5ra05912g
10.1039/c6ra26781e
10.1039/c7tc05245f
10.1039/c7cs00162b
10.1039/c4ra11264d
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Keywords STILBENE
2-PHOTON ABSORPTION
NONLINEAR-OPTICAL PROPERTIES
CONTINUUM
BIREFRINGENCE
DERIVATIVES
EFFICIENT
INTRAMOLECULAR CHARGE-TRANSFER
AZO-DYE
MOLECULES
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References Delaire (C9NJ00575G-(cit4)/*[position()=1]) 2000; 100
Larcher (C9NJ00575G-(cit12)/*[position()=1]) 2015; 7
Josse (C9NJ00575G-(cit16)/*[position()=1]) 2018; 6
Grabarz (C9NJ00575G-(cit27)/*[position()=1]) 2016; 81
Slama-Schwok (C9NJ00575G-(cit30)/*[position()=1]) 1990; 94
Varanasi (C9NJ00575G-(cit34)/*[position()=1]) 1996; 118
Mysliwiec (C9NJ00575G-(cit5)/*[position()=1]) 2011; 33
Ostroverkhova (C9NJ00575G-(cit1)/*[position()=1]) 2016; 116
Zhao (C9NJ00575G-(cit2)/*[position()=1]) 2008; 20
Chang (C9NJ00575G-(cit26)/*[position()=1]) 2008; 18
Ehrlich (C9NJ00575G-(cit32)/*[position()=1]) 1997; 22
Cheng (C9NJ00575G-(cit31)/*[position()=1]) 1991; 95
Fuks-Janczarek (C9NJ00575G-(cit42)/*[position()=1]) 2009; 9
Kulyk (C9NJ00575G-(cit19)/*[position()=1]) 2017; 145
Alain (C9NJ00575G-(cit25)/*[position()=1]) 1999; 245
Armand (C9NJ00575G-(cit14)/*[position()=1]) 2008; 451
Parafiniuk (C9NJ00575G-(cit9)/*[position()=1]) 2017; 19
Long (C9NJ00575G-(cit7)/*[position()=1]) 1995; 34
Bureš (C9NJ00575G-(cit46)/*[position()=1]) 2014; 4
Faurie (C9NJ00575G-(cit45)/*[position()=1]) 2018; 154
Jacquemin (C9NJ00575G-(cit53)/*[position()=1]) 2012; 14
Baig (C9NJ00575G-(cit48)/*[position()=1]) 2018; 3
Oudar (C9NJ00575G-(cit33)/*[position()=1]) 1977; 67
Singer (C9NJ00575G-(cit28)/*[position()=1]) 1989; 6
Tomasi (C9NJ00575G-(cit50)/*[position()=1]) 2005; 105
Persano (C9NJ00575G-(cit8)/*[position()=1]) 2014; 26
Caricato (C9NJ00575G-(cit51)/*[position()=1]) 2006; 124
Blanche (C9NJ00575G-(cit18)/*[position()=1]) 1999; 24
Szukalski (C9NJ00575G-(cit39)/*[position()=1]) 2017; 7
Santoro (C9NJ00575G-(cit56)/*[position()=1]) 2016; 6
Wu (C9NJ00575G-(cit20)/*[position()=1]) 2004; 37
Koynov (C9NJ00575G-(cit29)/*[position()=1]) 2005; 109
Consoli (C9NJ00575G-(cit10)/*[position()=1]) 2017; 7
Romaniello (C9NJ00575G-(cit35)/*[position()=1]) 2004; 125
Improta (C9NJ00575G-(cit36)/*[position()=1]) 2005; 109
Pawlicki (C9NJ00575G-(cit37)/*[position()=1]) 2009; 48
List (C9NJ00575G-(cit21)/*[position()=1]) 2015; 11
Szukalski (C9NJ00575G-(cit38)/*[position()=1]) 2016; 120
Ayadi (C9NJ00575G-(cit40)/*[position()=1]) 2017; 138
Yuan (C9NJ00575G-(cit44)/*[position()=1]) 2016; 120
Le Bahers (C9NJ00575G-(cit54)/*[position()=1]) 2011; 7
Arunkumar (C9NJ00575G-(cit6)/*[position()=1]) 2005
Zhai (C9NJ00575G-(cit13)/*[position()=1]) 2011; 23
Miertuš (C9NJ00575G-(cit49)/*[position()=1]) 1981; 55
Jou (C9NJ00575G-(cit11)/*[position()=1]) 2013; 23
Messier (C9NJ00575G-(cit3)/*[position()=1]) 1991
Roncali (C9NJ00575G-(cit17)/*[position()=1]) 2014; 26
Brédas (C9NJ00575G-(cit22)/*[position()=1]) 2004; 104
Jen (C9NJ00575G-(cit43)/*[position()=1]) 1997; 9
Medishetty (C9NJ00575G-(cit15)/*[position()=1]) 2017; 46
Gong (C9NJ00575G-(cit41)/*[position()=1]) 2006; 110
Chibani (C9NJ00575G-(cit52)/*[position()=1]) 2013; 4
Papagiannouli (C9NJ00575G-(cit23)/*[position()=1]) 2015; 5
Edvinsson (C9NJ00575G-(cit24)/*[position()=1]) 2007; 111
Li (C9NJ00575G-(cit47)/*[position()=1]) 2014; 53
Caricato, M (WOS:000236464000057) 2006; 124
Blanche, PA (WOS:000082832100009) 1999; 24
Consoli, A (WOS:000392230400001) 2017; 7
Varanasi, PR (WOS:A1996VX65400022) 1996; 118
Santoro, F (WOS:000382573700001) 2016; 6
LONG, NJ (WOS:A1995QC61000001) 1995; 34
Medishetty, R (WOS:000407635200009) 2017; 46
Wu, YL (WOS:000223160000040) 2004; 37
Faurie, A (WOS:000432501000006) 2018; 154
MIERTUS, S (WOS:A1981LD90200011) 1981; 55
Messier, J. (000468631600034.35) 1991
Gong, W (WOS:000237844900010) 2006; 110
Le Bahers, T (WOS:000293662500019) 2011; 7
Persano, L. (000468631600034.43) 2014; 26
Papagiannouli, I (WOS:000355738300025) 2015; 5
Parafiniuk, K (WOS:000405424100060) 2017; 19
Bures, F (WOS:000345460800094) 2014; 4
Szukalski, A (WOS:000379990400040) 2016; 120
Delaire, JA (WOS:000087009200008) 2000; 100
Grabarz, AM (WOS:000372664700007) 2016; 81
Jacquemin, D (WOS:000302062200007) 2012; 14
Zhao, YS (WOS:000258789200016) 2008; 20
Kulyk, B (WOS:000405972900029) 2017; 145
Baig, MZK (WOS:000444182900053) 2018; 3
Frisch, M. J. (000468631600034.18) 2016
Roncali, J (WOS:000337618600003) 2014; 26
Yuan, JY (WOS:000379990400043) 2016; 120
Pawlicki, M (WOS:000265740500008) 2009; 48
CHENG, LT (WOS:A1991GY16400026) 1991; 95
Jou, JH (WOS:000319824200011) 2013; 23
Alain, V (WOS:000082219000006) 1999; 245
Ostroverkhova, O (WOS:000388913000003) 2016; 116
Armand, M (WOS:000252929500029) 2008; 451
Tomasi, J (WOS:000231188700004) 2005; 105
Larcher, D (WOS:000346409400008) 2015; 7
Koynov, K (WOS:000229296600045) 2005; 109
Zhai, YP (WOS:000297042000001) 2011; 23
Jen, AKY (WOS:A1997WH74600005) 1997; 9
Chibani, S (WOS:000316966500003) 2013; 4
Ayadi, A (WOS:000392681700030) 2017; 138
Mysliwiec, J (WOS:000292425500004) 2011; 33
List, NH (WOS:000361087600023) 2015; 11
Josse, P (WOS:000423402500010) 2018; 6
Improta, R (WOS:000233342300019) 2005; 109
Romaniello, P (WOS:000188712100004) 2004; 125
Li, WL (WOS:000334894100016) 2014; 53
Arunkumar, E (WOS:000232322700002) 2005; 2005
SLAMASCHWOK, A (WOS:A1990DE69600007) 1990; 94
Fuks-Janczarek, I (WOS:000261360300035) 2009; 9
Ehrlich, JE (WOS:000071030800005) 1997; 22
Brédas, JL (WOS:000225082300004) 2004; 104
OUDAR, JL (WOS:A1977DP68500012) 1977; 67
SINGER, KD (WOS:A1989AD93200011) 1989; 6
Edvinsson, T (WOS:000250438900002) 2007; 111
Chang, YT (WOS:000258834600010) 2008; 18
Szukalski, A (WOS:000393761600069) 2017; 7
References_xml – issn: 2016
  publication-title: Gaussian 16 Rev. A.03
  doi: Frisch Trucks Schlegel Scuseria Robb Cheeseman Scalmani Barone Petersson Nakatsuji Li Caricato Marenich Bloino Janesko Gomperts Mennucci Hratchian Ortiz Izmaylov Sonnenberg Williams-Young Ding Lipparini Egidi Goings Peng Petrone Henderson Ranasinghe Zakrzewski Gao Rega Zheng Liang Hada Ehara Toyota Fukuda Hasegawa Ishida Nakajima Honda Kitao Nakai Vreven Throssell Montgomery Jr. Peralta Ogliaro Bearpark Heyd Brothers Kudin Staroverov Keith Kobayashi Normand Raghavachari Rendell Burant Iyengar Tomasi Cossi Millam Klene Adamo Cammi Ochterski Martin Morokuma Farkas Foresman Fox
– issn: 1991
  publication-title: Organic Molecules for Nonlinear Optics and Photonics
  doi: Messier Kajzar Prasad
– volume: 33
  start-page: 1382
  year: 2011
  ident: C9NJ00575G-(cit5)/*[position()=1]
  publication-title: Opt. Mater.
  doi: 10.1016/j.optmat.2011.02.034
– volume: 67
  start-page: 446
  year: 1977
  ident: C9NJ00575G-(cit33)/*[position()=1]
  publication-title: J. Chem. Phys.
  doi: 10.1063/1.434888
– volume: 125
  start-page: 145
  year: 2004
  ident: C9NJ00575G-(cit35)/*[position()=1]
  publication-title: J. Fluorine Chem.
  doi: 10.1016/j.jfluchem.2003.10.002
– volume: 23
  start-page: 2750
  year: 2013
  ident: C9NJ00575G-(cit11)/*[position()=1]
  publication-title: Adv. Funct. Mater.
  doi: 10.1002/adfm.201203209
– volume-title: Organic Molecules for Nonlinear Optics and Photonics
  year: 1991
  ident: C9NJ00575G-(cit3)/*[position()=1]
  doi: 10.1007/978-94-011-3370-8
– volume: 3
  start-page: 9114
  year: 2018
  ident: C9NJ00575G-(cit48)/*[position()=1]
  publication-title: ACS Omega
  doi: 10.1021/acsomega.8b01258
– volume: 116
  start-page: 13279
  year: 2016
  ident: C9NJ00575G-(cit1)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.6b00127
– volume: 124
  start-page: 124520
  year: 2006
  ident: C9NJ00575G-(cit51)/*[position()=1]
  publication-title: J. Chem. Phys.
  doi: 10.1063/1.2183309
– volume: 5
  start-page: 48363
  year: 2015
  ident: C9NJ00575G-(cit23)/*[position()=1]
  publication-title: RSC Adv.
  doi: 10.1039/C5RA05912G
– volume: 4
  start-page: 58826
  year: 2014
  ident: C9NJ00575G-(cit46)/*[position()=1]
  publication-title: RSC Adv.
  doi: 10.1039/C4RA11264D
– volume: 95
  start-page: 10631
  year: 1991
  ident: C9NJ00575G-(cit31)/*[position()=1]
  publication-title: J. Phys. Chem.
  doi: 10.1021/j100179a026
– volume: 4
  start-page: 1950
  year: 2013
  ident: C9NJ00575G-(cit52)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/c3sc22265a
– volume: 138
  start-page: 255
  year: 2017
  ident: C9NJ00575G-(cit40)/*[position()=1]
  publication-title: Dyes Pigm.
  doi: 10.1016/j.dyepig.2016.11.030
– volume: 14
  start-page: 5383
  year: 2012
  ident: C9NJ00575G-(cit53)/*[position()=1]
  publication-title: Phys. Chem. Chem. Phys.
  doi: 10.1039/c2cp40261k
– volume: 46
  start-page: 4976
  year: 2017
  ident: C9NJ00575G-(cit15)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C7CS00162B
– volume: 145
  start-page: 256
  year: 2017
  ident: C9NJ00575G-(cit19)/*[position()=1]
  publication-title: Dyes Pigm.
  doi: 10.1016/j.dyepig.2017.06.012
– volume: 110
  start-page: 10241
  year: 2006
  ident: C9NJ00575G-(cit41)/*[position()=1]
  publication-title: J. Phys. Chem. B
  doi: 10.1021/jp055449z
– volume: 7
  start-page: 19
  year: 2015
  ident: C9NJ00575G-(cit12)/*[position()=1]
  publication-title: Nat. Chem.
  doi: 10.1038/nchem.2085
– volume: 105
  start-page: 2999
  year: 2005
  ident: C9NJ00575G-(cit50)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/cr9904009
– volume: 48
  start-page: 3244
  year: 2009
  ident: C9NJ00575G-(cit37)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200805257
– volume: 19
  start-page: 18068
  year: 2017
  ident: C9NJ00575G-(cit9)/*[position()=1]
  publication-title: Phys. Chem. Chem. Phys.
  doi: 10.1039/C7CP02249B
– volume: 120
  start-page: 14813
  year: 2016
  ident: C9NJ00575G-(cit38)/*[position()=1]
  publication-title: J. Phys. Chem. C
  doi: 10.1021/acs.jpcc.6b03915
– volume: 118
  start-page: 12443
  year: 1996
  ident: C9NJ00575G-(cit34)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja960136q
– volume: 9
  start-page: 484
  year: 2009
  ident: C9NJ00575G-(cit42)/*[position()=1]
  publication-title: Curr. Appl. Phys.
  doi: 10.1016/j.cap.2008.04.010
– volume: 6
  start-page: 761
  year: 2018
  ident: C9NJ00575G-(cit16)/*[position()=1]
  publication-title: J. Mater. Chem. C
  doi: 10.1039/C7TC05245F
– volume: 9
  start-page: 132
  year: 1997
  ident: C9NJ00575G-(cit43)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/adma.19970090207
– volume: 53
  start-page: 4603
  year: 2014
  ident: C9NJ00575G-(cit47)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201310438
– volume: 100
  start-page: 1817
  year: 2000
  ident: C9NJ00575G-(cit4)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/cr980078m
– volume: 154
  start-page: 38
  year: 2018
  ident: C9NJ00575G-(cit45)/*[position()=1]
  publication-title: Dyes Pigm.
  doi: 10.1016/j.dyepig.2018.02.025
– volume: 7
  start-page: 2498
  year: 2011
  ident: C9NJ00575G-(cit54)/*[position()=1]
  publication-title: J. Chem. Theory Comput.
  doi: 10.1021/ct200308m
– start-page: 4051
  year: 2005
  ident: C9NJ00575G-(cit6)/*[position()=1]
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.200500372
– volume: 20
  start-page: 2859
  year: 2008
  ident: C9NJ00575G-(cit2)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/adma.200800604
– volume: 26
  start-page: 3821
  year: 2014
  ident: C9NJ00575G-(cit17)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/adma.201305999
– volume: 22
  start-page: 1843
  year: 1997
  ident: C9NJ00575G-(cit32)/*[position()=1]
  publication-title: Opt. Lett.
  doi: 10.1364/OL.22.001843
– volume: 26
  start-page: 6660
  year: 2014
  ident: C9NJ00575G-(cit8)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/adma.201470263
– volume: 451
  start-page: 652
  year: 2008
  ident: C9NJ00575G-(cit14)/*[position()=1]
  publication-title: Nature
  doi: 10.1038/451652a
– volume: 6
  start-page: 1339
  year: 1989
  ident: C9NJ00575G-(cit28)/*[position()=1]
  publication-title: J. Opt. Soc. Am. B
  doi: 10.1364/JOSAB.6.001339
– volume: 109
  start-page: 10058
  year: 2005
  ident: C9NJ00575G-(cit36)/*[position()=1]
  publication-title: J. Phys. Chem. A
  doi: 10.1021/jp054250j
– volume: 34
  start-page: 21
  year: 1995
  ident: C9NJ00575G-(cit7)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed. Engl.
  doi: 10.1002/anie.199500211
– volume: 11
  start-page: 4182
  year: 2015
  ident: C9NJ00575G-(cit21)/*[position()=1]
  publication-title: J. Chem. Theory Comput.
  doi: 10.1021/acs.jctc.5b00538
– volume: 37
  start-page: 6090
  year: 2004
  ident: C9NJ00575G-(cit20)/*[position()=1]
  publication-title: Macromolecules
  doi: 10.1021/ma0493980
– volume: 7
  start-page: 40141
  year: 2017
  ident: C9NJ00575G-(cit10)/*[position()=1]
  publication-title: Sci. Rep.
  doi: 10.1038/srep40141
– volume: 81
  start-page: 2280
  year: 2016
  ident: C9NJ00575G-(cit27)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.5b02691
– volume: 104
  start-page: 4971
  year: 2004
  ident: C9NJ00575G-(cit22)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/cr040084k
– volume: 94
  start-page: 3894
  year: 1990
  ident: C9NJ00575G-(cit30)/*[position()=1]
  publication-title: J. Phys. Chem.
  doi: 10.1021/j100373a007
– volume: 23
  start-page: 4828
  year: 2011
  ident: C9NJ00575G-(cit13)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/adma.201100984
– volume: 7
  start-page: 9941
  year: 2017
  ident: C9NJ00575G-(cit39)/*[position()=1]
  publication-title: RSC Adv.
  doi: 10.1039/C6RA26781E
– volume: 245
  start-page: 51
  year: 1999
  ident: C9NJ00575G-(cit25)/*[position()=1]
  publication-title: Chem. Phys.
  doi: 10.1016/S0301-0104(99)00073-7
– volume: 55
  start-page: 117
  year: 1981
  ident: C9NJ00575G-(cit49)/*[position()=1]
  publication-title: Chem. Phys.
  doi: 10.1016/0301-0104(81)85090-2
– volume: 18
  start-page: 2356
  year: 2008
  ident: C9NJ00575G-(cit26)/*[position()=1]
  publication-title: Adv. Funct. Mater.
  doi: 10.1002/adfm.200701150
– volume: 120
  start-page: 14840
  year: 2016
  ident: C9NJ00575G-(cit44)/*[position()=1]
  publication-title: J. Phys. Chem. C
  doi: 10.1021/acs.jpcc.6b04849
– volume: 24
  start-page: 1349
  year: 1999
  ident: C9NJ00575G-(cit18)/*[position()=1]
  publication-title: Opt. Lett.
  doi: 10.1364/OL.24.001349
– volume: 109
  start-page: 10184
  year: 2005
  ident: C9NJ00575G-(cit29)/*[position()=1]
  publication-title: J. Phys. Chem. B
  doi: 10.1021/jp0508913
– volume: 6
  start-page: 460
  year: 2016
  ident: C9NJ00575G-(cit56)/*[position()=1]
  publication-title: Wiley Interdiscip. Rev.: Comput. Mol. Sci.
– volume: 111
  start-page: 15137
  year: 2007
  ident: C9NJ00575G-(cit24)/*[position()=1]
  publication-title: J. Phys. Chem. C
  doi: 10.1021/jp076447c
– volume: 22
  start-page: 1843
  year: 1997
  ident: WOS:000071030800005
  article-title: Two-photon absorption and broadband optical limiting with bis-donor stilbenes
  publication-title: OPTICS LETTERS
– volume: 124
  start-page: ARTN 124520
  year: 2006
  ident: WOS:000236464000057
  article-title: Formation and relaxation of excited states in solution: A new time dependent polarizable continuum model based on time dependent density functional theory
  publication-title: JOURNAL OF CHEMICAL PHYSICS
  doi: 10.1063/1.2183309
– volume: 33
  start-page: 1382
  year: 2011
  ident: WOS:000292425500004
  article-title: Pulsed laser induced birefringence switching in a biopolymer matrix containing azo-dye molecules
  publication-title: OPTICAL MATERIALS
  doi: 10.1016/j.optmat.2011.02.034
– volume: 138
  start-page: 255
  year: 2017
  ident: WOS:000392681700030
  article-title: TTF based donor-pi-acceptor dyads synthesized for NLO applications
  publication-title: DYES AND PIGMENTS
  doi: 10.1016/j.dyepig.2016.11.030
– volume: 11
  start-page: 4182
  year: 2015
  ident: WOS:000361087600023
  article-title: Relation between Nonlinear Optical Properties of Push-Pull Molecules and Metric of Charge Transfer Excitations
  publication-title: JOURNAL OF CHEMICAL THEORY AND COMPUTATION
  doi: 10.1021/acs.jctc.5b00538
– volume: 94
  start-page: 3894
  year: 1990
  ident: WOS:A1990DE69600007
  article-title: INTRAMOLECULAR CHARGE-TRANSFER IN DONOR-ACCEPTOR MOLECULES
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY
– volume: 24
  start-page: 1349
  year: 1999
  ident: WOS:000082832100009
  article-title: Photoinduced orientation of azo dye in various polymer matrices
  publication-title: OPTICS LETTERS
– volume: 23
  start-page: 4828
  year: 2011
  ident: WOS:000297042000001
  article-title: Carbon Materials for Chemical Capacitive Energy Storage
  publication-title: ADVANCED MATERIALS
  doi: 10.1002/adma.201100984
– volume: 95
  start-page: 10631
  year: 1991
  ident: WOS:A1991GY16400026
  article-title: EXPERIMENTAL INVESTIGATIONS OF ORGANIC MOLECULAR NONLINEAR OPTICAL POLARIZABILITIES .1. METHODS AND RESULTS ON BENZENE AND STILBENE DERIVATIVES
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY
– volume: 7
  start-page: ARTN 40141
  year: 2017
  ident: WOS:000392230400001
  article-title: Lasing optical cavities based on macroscopic scattering elements
  publication-title: SCIENTIFIC REPORTS
  doi: 10.1038/srep40141
– volume: 104
  start-page: 4971
  year: 2004
  ident: WOS:000225082300004
  article-title: Charge-transfer and energy-transfer processes in π-conjugated oligomers and polymers:: A molecular picture
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr040084k
– volume: 26
  start-page: 3821
  year: 2014
  ident: WOS:000337618600003
  article-title: Molecular Materials for Organic Photovoltaics: Small is Beautiful
  publication-title: ADVANCED MATERIALS
  doi: 10.1002/adma.201305999
– volume: 6
  start-page: 460
  year: 2016
  ident: WOS:000382573700001
  article-title: Going beyond the vertical approximation with time-dependent density functional theory
  publication-title: WILEY INTERDISCIPLINARY REVIEWS-COMPUTATIONAL MOLECULAR SCIENCE
  doi: 10.1002/wcms.1260
– volume: 4
  start-page: 1950
  year: 2013
  ident: WOS:000316966500003
  article-title: Revisiting the optical signatures of BODIPY with ab initio tools
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c3sc22265a
– volume: 109
  start-page: 10058
  year: 2005
  ident: WOS:000233342300019
  article-title: Excited-state behavior of trans and cis isomers of stilbene and stiff stilbene: A TD-DFT study
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY A
  doi: 10.1021/jp054250j
– year: 1991
  ident: 000468631600034.35
  publication-title: Organic Molecules for Nonlinear Optics and Photonics
– volume: 19
  start-page: 18068
  year: 2017
  ident: WOS:000405424100060
  article-title: Enlargement of the organic solid-state DFB laser wavelength tuning range by the use of two complementary luminescent dyes doped into the host matrix
  publication-title: PHYSICAL CHEMISTRY CHEMICAL PHYSICS
  doi: 10.1039/c7cp02249b
– volume: 111
  start-page: 15137
  year: 2007
  ident: WOS:000250438900002
  article-title: Intramolecular charge-transfer tuning of perylenes:: Spectroscopic features and performance in Dye-sensitized solar cells
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY C
  doi: 10.1021/jp076447c
– volume: 23
  start-page: 2750
  year: 2013
  ident: WOS:000319824200011
  article-title: Candle Light-Style Organic Light-Emitting Diodes
  publication-title: ADVANCED FUNCTIONAL MATERIALS
  doi: 10.1002/adfm.201203209
– volume: 100
  start-page: 1817
  year: 2000
  ident: WOS:000087009200008
  article-title: Linear and nonlinear optical properties of photochromic molecules and materials
  publication-title: CHEMICAL REVIEWS
– volume: 67
  start-page: 446
  year: 1977
  ident: WOS:A1977DP68500012
  article-title: OPTICAL NONLINEARITIES OF CONJUGATED MOLECULES - STILBENE DERIVATIVES AND HIGHLY POLAR AROMATIC-COMPOUNDS
  publication-title: JOURNAL OF CHEMICAL PHYSICS
– volume: 120
  start-page: 14840
  year: 2016
  ident: WOS:000379990400043
  article-title: Spirooxazine-Fulgide Biphotochromic Molecular Switches with Nonlinear Optical Responses across Four States
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY C
  doi: 10.1021/acs.jpcc.6b04849
– volume: 105
  start-page: 2999
  year: 2005
  ident: WOS:000231188700004
  article-title: Quantum mechanical continuum solvation models
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr9904009
– volume: 81
  start-page: 2280
  year: 2016
  ident: WOS:000372664700007
  article-title: The Influence of the π-Conjugated Spacer on Photophysical Properties of Difluoroboranyls Derived from Amides Carrying a Donor Group
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.5b02691
– volume: 451
  start-page: 652
  year: 2008
  ident: WOS:000252929500029
  article-title: Building better batteries
  publication-title: NATURE
  doi: 10.1038/451652a
– volume: 34
  start-page: 21
  year: 1995
  ident: WOS:A1995QC61000001
  article-title: ORGANOMETALLIC COMPOUNDS FOR NONLINEAR OPTICS - THE SEARCH FOR EN-LIGHT-ENMENT
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
– volume: 116
  start-page: 13279
  year: 2016
  ident: WOS:000388913000003
  article-title: Organic Optoelectronic Materials: Mechanisms and Applications
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.6b00127
– volume: 7
  start-page: 19
  year: 2015
  ident: WOS:000346409400008
  article-title: Towards greener and more sustainable batteries for electrical energy storage
  publication-title: NATURE CHEMISTRY
  doi: 10.1038/NCHEM.2085
– volume: 5
  start-page: 48363
  year: 2015
  ident: WOS:000355738300025
  article-title: Pyrazoline derivatives with a tailored third order nonlinear optical response
  publication-title: RSC ADVANCES
  doi: 10.1039/c5ra05912g
– volume: 9
  start-page: 484
  year: 2009
  ident: WOS:000261360300035
  article-title: Specific features of nonlinear optical effects in several stilbene derivatives
  publication-title: CURRENT APPLIED PHYSICS
  doi: 10.1016/j.cap.2008.04.010
– volume: 154
  start-page: 38
  year: 2018
  ident: WOS:000432501000006
  article-title: Facile synthesis and optical properties of extended TPA-Benzodifuran derivatives connected by cyano-vinylene junctions
  publication-title: DYES AND PIGMENTS
  doi: 10.1016/j.dyepig.2018.02.025
– volume: 245
  start-page: 51
  year: 1999
  ident: WOS:000082219000006
  article-title: Elongated push-pull diphenylpolyenes for nonlinear optics:: molecular engineering of quadratic and cubic optical nonlinearities via tuning of intramolecular charge transfer
  publication-title: CHEMICAL PHYSICS
– volume: 125
  start-page: 145
  year: 2004
  ident: WOS:000188712100004
  article-title: Effects of fluorine atoms on the optical nonlinear response of stilbene derivatives
  publication-title: JOURNAL OF FLUORINE CHEMISTRY
  doi: 10.1016/j.jfluchem.2003.10.002
– volume: 55
  start-page: 117
  year: 1981
  ident: WOS:A1981LD90200011
  article-title: ELECTROSTATIC INTERACTION OF A SOLUTE WITH A CONTINUUM - A DIRECT UTILIZATION OF ABINITIO MOLECULAR POTENTIALS FOR THE PREVISION OF SOLVENT EFFECTS
  publication-title: CHEMICAL PHYSICS
– volume: 7
  start-page: 9941
  year: 2017
  ident: WOS:000393761600069
  article-title: Chemical structure versus second-order nonlinear optical response of the push-pull type pyrazoline-based chromophores
  publication-title: RSC ADVANCES
  doi: 10.1039/c6ra26781e
– volume: 53
  start-page: 4603
  year: 2014
  ident: WOS:000334894100016
  article-title: Separation of Photoactive Conformers Based on Hindered Diarylethenes: Efficient Modulation in Photocyclization Quantum Yields
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201310438
– volume: 120
  start-page: 14813
  year: 2016
  ident: WOS:000379990400040
  article-title: Photo-Physical Transformations in Pyrazoline Derivative Based Systems
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY C
  doi: 10.1021/acs.jpcc.6b03915
– volume: 6
  start-page: 1339
  year: 1989
  ident: WOS:A1989AD93200011
  article-title: 2ND-ORDER NONLINEAR-OPTICAL PROPERTIES OF DONOR-SUBSTITUTED AND ACCEPTOR-SUBSTITUTED AROMATIC-COMPOUNDS
  publication-title: JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS
– volume: 118
  start-page: 12443
  year: 1996
  ident: WOS:A1996VX65400022
  article-title: The important role of heteroaromatics in the design of efficient second-order nonlinear optical molecules: Theoretical investigation on push-pull heteroaromatic stilbenes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 2005
  start-page: 4051
  year: 2005
  ident: WOS:000232322700002
  article-title: Improving the properties of organic dyes by molecular encapsulation
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.200500372
– volume: 18
  start-page: 2356
  year: 2008
  ident: WOS:000258834600010
  article-title: Intramolecular donor-acceptor regioregular poly(3-hexylthiophene)s presenting octylphenanthrenyl-imidazole moieties exhibit enhanced charge transfer for heterojunction solar cell applications
  publication-title: ADVANCED FUNCTIONAL MATERIALS
  doi: 10.1002/adfm.200701150
– volume: 145
  start-page: 256
  year: 2017
  ident: WOS:000405972900029
  article-title: Functionalized azo-based iminopyridine rhenium complexes for nonlinear optical performance
  publication-title: DYES AND PIGMENTS
  doi: 10.1016/j.dyepig.2017.06.012
– volume: 6
  start-page: 761
  year: 2018
  ident: WOS:000423402500010
  article-title: Bromination of the benzothioxanthene Bloc: toward new π-conjugated systems for organic electronic applications
  publication-title: JOURNAL OF MATERIALS CHEMISTRY C
  doi: 10.1039/c7tc05245f
– volume: 46
  start-page: 4976
  year: 2017
  ident: WOS:000407635200009
  article-title: Nonlinear optical properties, upconversion and lasing in metal-organic frameworks
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c7cs00162b
– volume: 109
  start-page: 10184
  year: 2005
  ident: WOS:000229296600045
  article-title: Effect of donor-acceptor substitution on the nonlinear optical properties of oligo(1,4-phenyleneethynylene)s studied by third harmonic generation spectroscopy
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY B
  doi: 10.1021/jp0508913
– volume: 9
  start-page: 132
  year: 1997
  ident: WOS:A1997WH74600005
  article-title: Synthesis and characterization of highly efficient and thermally stable diphenylamino-substituted thiophene stilbene chromophores for nonlinear optical applications
  publication-title: ADVANCED MATERIALS
– volume: 3
  start-page: 9114
  year: 2018
  ident: WOS:000444182900053
  article-title: Weak Donor-/Strong Acceptor-Linked Anthracenyl π-Conjugates as Solvato(fluoro)chromophore and AEEgens: Contrast between Nitro and Cyano Functionality
  publication-title: ACS OMEGA
  doi: 10.1021/acsomega.8b01258
– volume: 20
  start-page: 2859
  year: 2008
  ident: WOS:000258789200016
  article-title: Low-dimensional nanomaterials based on small organic molecules: Preparation and optoelectronic properties
  publication-title: ADVANCED MATERIALS
  doi: 10.1002/adma.200800604
– volume: 7
  start-page: 2498
  year: 2011
  ident: WOS:000293662500019
  article-title: A Qualitative Index of Spatial Extent in Charge-Transfer Excitations
  publication-title: JOURNAL OF CHEMICAL THEORY AND COMPUTATION
  doi: 10.1021/ct200308m
– volume: 26
  start-page: 6660
  year: 2014
  ident: 000468631600034.43
  publication-title: Adv. Mater.
– year: 2016
  ident: 000468631600034.18
  publication-title: Gaussian 16 Rev. A.03
– volume: 48
  start-page: 3244
  year: 2009
  ident: WOS:000265740500008
  article-title: Two-Photon Absorption and the Design of Two-Photon Dyes
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200805257
– volume: 110
  start-page: 10241
  year: 2006
  ident: WOS:000237844900010
  article-title: Synthesis and characterization of indole-containing chromophores for second-order nonlinear optics
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY B
  doi: 10.1021/jp055449z
– volume: 14
  start-page: 5383
  year: 2012
  ident: WOS:000302062200007
  article-title: What is the "best" atomic charge model to describe through-space charge-transfer excitations?
  publication-title: PHYSICAL CHEMISTRY CHEMICAL PHYSICS
  doi: 10.1039/c2cp40261k
– volume: 4
  start-page: 58826
  year: 2014
  ident: WOS:000345460800094
  article-title: Fundamental aspects of property tuning in push-pull molecules
  publication-title: RSC ADVANCES
  doi: 10.1039/c4ra11264d
– volume: 37
  start-page: 6090
  year: 2004
  ident: WOS:000223160000040
  article-title: Photoinduced birefringence and surface relief gratings in polyurethane elastomers with azobenzene chromophore in the hard segment
  publication-title: MACROMOLECULES
  doi: 10.1021/ma0493980
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Snippet In this paper we report the synthesis and photophysical properties of six novel thiophene derivatives (ThD) with D-π-A structure. The subject of this work is...
In this paper we report the synthesis and photophysical properties of six novel thiophene derivatives (ThD) with D–π–A structure. The subject of this work is...
In this paper we report the synthesis and photophysical properties of six novel thiophene derivatives (ThD) with D--A structure. The subject of this work is...
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SubjectTerms Aromatic compounds
Carbon 13
Charge transfer
Chemical Sciences
Chemical synthesis
Chemistry
Chemistry, Multidisciplinary
Chromophores
Emission spectra
Fluorescence
Mass spectrometry
Mathematical analysis
Nitrogen dioxide
NMR
Nuclear magnetic resonance
Optical properties
Organic chemistry
Photoluminescence
Physical Sciences
Quantum chemistry
Science & Technology
Title Tunable photophysical properties of thiophene based chromophores: a conjoined experimental and theoretical investigation
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Volume 43
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