A general strategy for development of a single benzene fluorophore with full-color-tunable, environmentally insensitive, and two-photon solid-state emission
We report here a single-benzene based fluorescent framework, amino-terephthalonitrile, denoted SB-Fluor . This scaffold displays versatile emission wavelength tunability via structure modification, covering the full visible light spectrum, both in the solution and solid state. Moreover, one molecule...
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Published in | Chemical communications (Cambridge, England) Vol. 55; no. 76; pp. 11462 - 11465 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
CAMBRIDGE
Royal Soc Chemistry
19.09.2019
Royal Society of Chemistry |
Subjects | |
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Abstract | We report here a single-benzene based fluorescent framework, amino-terephthalonitrile, denoted
SB-Fluor
. This scaffold displays versatile emission wavelength tunability
via
structure modification, covering the full visible light spectrum, both in the solution and solid state. Moreover, one molecule, SBF3, exhibits polymorphism-dependent reversible mechanochromic luminescence.
We report here a single-benzene based fluorescent framework, amino-terephthalonitrile, denoted
SB-Fluor
. |
---|---|
AbstractList | We report here a single-benzene based fluorescent framework, amino-terephthalonitrile, denoted SB-Fluor. This scaffold displays versatile emission wavelength tunability via structure modification, covering the full visible light spectrum, both in the solution and solid state. Moreover, one molecule, SBF3, exhibits polymorphism-dependent reversible mechanochromic luminescence. We report here a single-benzene based fluorescent framework, amino-terephthalonitrile, denoted SB-Fluor. This scaffold displays versatile emission wavelength tunability via structure modification, covering the full visible light spectrum, both in the solution and solid state. Moreover, one molecule, SBF3, exhibits polymorphism-dependent reversible mechanochromic luminescence.We report here a single-benzene based fluorescent framework, amino-terephthalonitrile, denoted SB-Fluor. This scaffold displays versatile emission wavelength tunability via structure modification, covering the full visible light spectrum, both in the solution and solid state. Moreover, one molecule, SBF3, exhibits polymorphism-dependent reversible mechanochromic luminescence. We report here a single-benzene based fluorescent framework, amino-terephthalonitrile, denoted SB-Fluor . This scaffold displays versatile emission wavelength tunability via structure modification, covering the full visible light spectrum, both in the solution and solid state. Moreover, one molecule, SBF3, exhibits polymorphism-dependent reversible mechanochromic luminescence. We report here a single-benzene based fluorescent framework, amino-terephthalonitrile, denoted SB-Fluor . We report here a single-benzene based fluorescent framework, amino-terephthalonitrile, denoted SB-Fluor . This scaffold displays versatile emission wavelength tunability via structure modification, covering the full visible light spectrum, both in the solution and solid state. Moreover, one molecule, SBF3, exhibits polymorphism-dependent reversible mechanochromic luminescence. |
Author | Zhang, Xing-Xing Xiang, Zhen Ren, Tian-Bing Xu, Wang Yuan, Lin Liu, Yu-Peng Zhang, Xiao-Bing Wang, Zhi-Yao Wu, Peng |
AuthorAffiliation | Analytical & Testing Center and College of Chemistry Sichuan University College of Chemistry and Chemical Engineering State Key Laboratory of Chemo/Biosensing and Chemometrics Hunan University |
AuthorAffiliation_xml | – sequence: 0 name: State Key Laboratory of Chemo/Biosensing and Chemometrics – sequence: 0 name: Analytical & Testing Center and College of Chemistry – sequence: 0 name: College of Chemistry and Chemical Engineering – sequence: 0 name: Hunan University – sequence: 0 name: Sichuan University |
Author_xml | – sequence: 1 givenname: Zhen surname: Xiang fullname: Xiang, Zhen – sequence: 2 givenname: Zhi-Yao surname: Wang fullname: Wang, Zhi-Yao – sequence: 3 givenname: Tian-Bing surname: Ren fullname: Ren, Tian-Bing – sequence: 4 givenname: Wang surname: Xu fullname: Xu, Wang – sequence: 5 givenname: Yu-Peng surname: Liu fullname: Liu, Yu-Peng – sequence: 6 givenname: Xing-Xing surname: Zhang fullname: Zhang, Xing-Xing – sequence: 7 givenname: Peng surname: Wu fullname: Wu, Peng – sequence: 8 givenname: Lin surname: Yuan fullname: Yuan, Lin – sequence: 9 givenname: Xiao-Bing surname: Zhang fullname: Zhang, Xiao-Bing |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31490473$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1038/ncomms3061 10.1021/ja110766a 10.1039/C5SC01076D 10.1039/c1cs15113d 10.1039/C6CP05153G 10.1002/anie.201902264 10.1002/anie.201703439 10.1021/cb500078u 10.1038/17989 10.1021/cr990322p 10.1021/cb700248m 10.1002/adfm.201807623 10.1021/cr990402t 10.1002/anie.201710688 10.1021/cr900263j 10.1039/C8SC01635F 10.1038/ncomms11964 10.1021/jp902962h 10.1002/anie.201800293 10.1021/jacs.6b03924 10.1002/anie.201900465 10.1002/adma.201401356 10.1021/cr5004425 10.1038/nmeth.3256 10.1021/acs.analchem.9b00224 10.1021/jacs.5b03548 10.1002/anie.201712949 10.1021/acs.analchem.7b02538 10.1021/jacs.8b04404 10.1002/anie.201502365 10.1016/j.dyepig.2017.10.002 10.1002/anie.201706517 10.1039/c6cp05153g 10.1039/c8sc01635f 10.1039/c5sc01076d 10.1038/NMETH.3256 |
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References | Singha (C9CC06260B-(cit19)/*[position()=1]) 2015; 6 Tang (C9CC06260B-(cit22)/*[position()=1]) 2017; 56 Beppu (C9CC06260B-(cit21)/*[position()=1]) 2015; 54 Lavis (C9CC06260B-(cit16)/*[position()=1]) 2014; 9 Alamudi (C9CC06260B-(cit4)/*[position()=1]) 2016; 7 Watson (C9CC06260B-(cit10)/*[position()=1]) 2001; 101 Hu (C9CC06260B-(cit25)/*[position()=1]) 2009; 113 Hu (C9CC06260B-(cit31)/*[position()=1]) 2018; 149 Kim (C9CC06260B-(cit2)/*[position()=1]) 2011; 133 Sanyal (C9CC06260B-(cit27)/*[position()=1]) 2016; 18 Duan (C9CC06260B-(cit32)/*[position()=1]) 2019; 91 Ren (C9CC06260B-(cit6)/*[position()=1]) 2018; 140 Hu (C9CC06260B-(cit28)/*[position()=1]) 2019; 58 Benson (C9CC06260B-(cit14)/*[position()=1]) 2019; 58 Kobayashi (C9CC06260B-(cit24)/*[position()=1]) 2010; 110 Cumpston (C9CC06260B-(cit7)/*[position()=1]) 1999; 398 Mishra (C9CC06260B-(cit18)/*[position()=1]) 2000; 100 Zampetti (C9CC06260B-(cit9)/*[position()=1]) 2019; 29 Lavis (C9CC06260B-(cit1)/*[position()=1]) 2008; 3 Ren (C9CC06260B-(cit23)/*[position()=1]) 2017; 89 Mei (C9CC06260B-(cit17)/*[position()=1]) 2014; 26 Sun (C9CC06260B-(cit29)/*[position()=1]) 2017; 56 Chen (C9CC06260B-(cit15)/*[position()=1]) 2017; 56 Hong (C9CC06260B-(cit13)/*[position()=1]) 2011; 40 Gu (C9CC06260B-(cit26)/*[position()=1]) 2018; 9 Wang (C9CC06260B-(cit30)/*[position()=1]) 2018; 57 Ren (C9CC06260B-(cit5)/*[position()=1]) 2018; 57 Kim (C9CC06260B-(cit20)/*[position()=1]) 2015; 137 Grimm (C9CC06260B-(cit3)/*[position()=1]) 2015; 12 Liu (C9CC06260B-(cit12)/*[position()=1]) 2016; 138 Kim (C9CC06260B-(cit11)/*[position()=1]) 2015; 115 Gan (C9CC06260B-(cit8)/*[position()=1]) 2013; 4 Lavis, LD (WOS:000254218800003) 2008; 3 Hu, Q (WOS:000423246900028) 2018; 149 Singha, S (WOS:000356176200085) 2015; 6 Benson, S (WOS:000476423300011) 2019; 58 Ren, TB (WOS:000434949200034) 2018; 57 Tang, BL (WOS:000411810600020) 2017; 56 Duan, C (WOS:000462098300056) 2019; 91 Hu, RR (WOS:000269654700012) 2009; 113 Kim, E (WOS:000290363400031) 2011; 133 Liu, XG (WOS:000377643300014) 2016; 138 Ren, TB (WOS:000436211600053) 2018; 140 Lavis, LD (WOS:000334823200003) 2014; 9 Alamudi, SH (WOS:000379086400001) 2016; 7 Kim, HM (WOS:000356316300009) 2015; 115 Kobayashi, H (WOS:000277811600003) 2010; 110 Mei, J (WOS:000340680700008) 2014; 26 Hong, YN (WOS:000295921500012) 2011; 40 Gan, ZS (WOS:000323668400004) 2013; 4 Zampetti, A (WOS:000473101200006) 2019; 29 Chen, W (WOS:000418359400035) 2017; 56 Ren, TB (WOS:000414887000040) 2017; 89 Beppu, T (WOS:000356390300019) 2015; 54 Hu, J (WOS:000476608700019) 2019; 58 Kim, D (WOS:000355890600013) 2015; 137 Sun, LJ (WOS:000403839000024) 2017; 56 Cumpston, BH (WOS:000079033900047) 1999; 398 Sanyal, S (WOS:000385180600056) 2016; 18 Mishra, A (WOS:000087778100003) 2000; 100 Grimm, JB (WOS:000350670300026) 2015; 12 Gu, YA (WOS:000442262400005) 2018; 9 Wang, Y (WOS:000428350200016) 2018; 57 Watson, MD (WOS:000168684700008) 2001; 101 |
References_xml | – volume: 4 start-page: 2061 year: 2013 ident: C9CC06260B-(cit8)/*[position()=1] publication-title: Nat. Commun. doi: 10.1038/ncomms3061 – volume: 133 start-page: 6642 year: 2011 ident: C9CC06260B-(cit2)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja110766a – volume: 6 start-page: 4335 year: 2015 ident: C9CC06260B-(cit19)/*[position()=1] publication-title: Chem. Sci. doi: 10.1039/C5SC01076D – volume: 40 start-page: 5361 year: 2011 ident: C9CC06260B-(cit13)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/c1cs15113d – volume: 18 start-page: 28198 year: 2016 ident: C9CC06260B-(cit27)/*[position()=1] publication-title: Phys. Chem. Chem. Phys. doi: 10.1039/C6CP05153G – volume: 58 start-page: 8405 year: 2019 ident: C9CC06260B-(cit28)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201902264 – volume: 56 start-page: 7831 year: 2017 ident: C9CC06260B-(cit29)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201703439 – volume: 9 start-page: 855 year: 2014 ident: C9CC06260B-(cit16)/*[position()=1] publication-title: ACS Chem. Biol. doi: 10.1021/cb500078u – volume: 398 start-page: 51 year: 1999 ident: C9CC06260B-(cit7)/*[position()=1] publication-title: Nature doi: 10.1038/17989 – volume: 101 start-page: 1267 year: 2001 ident: C9CC06260B-(cit10)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr990322p – volume: 3 start-page: 142 year: 2008 ident: C9CC06260B-(cit1)/*[position()=1] publication-title: ACS Chem. Biol. doi: 10.1021/cb700248m – volume: 29 start-page: 1807623 year: 2019 ident: C9CC06260B-(cit9)/*[position()=1] publication-title: Adv. Funct. Mater. doi: 10.1002/adfm.201807623 – volume: 100 start-page: 1973 year: 2000 ident: C9CC06260B-(cit18)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr990402t – volume: 56 start-page: 16611 year: 2017 ident: C9CC06260B-(cit15)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201710688 – volume: 110 start-page: 2620 year: 2010 ident: C9CC06260B-(cit24)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr900263j – volume: 9 start-page: 6497 year: 2018 ident: C9CC06260B-(cit26)/*[position()=1] publication-title: Chem. Sci. doi: 10.1039/C8SC01635F – volume: 7 start-page: 11964 year: 2016 ident: C9CC06260B-(cit4)/*[position()=1] publication-title: Nat. Commun. doi: 10.1038/ncomms11964 – volume: 113 start-page: 15845 year: 2009 ident: C9CC06260B-(cit25)/*[position()=1] publication-title: J. Phys. Chem. C doi: 10.1021/jp902962h – volume: 57 start-page: 7473 year: 2018 ident: C9CC06260B-(cit5)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201800293 – volume: 138 start-page: 6960 year: 2016 ident: C9CC06260B-(cit12)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.6b03924 – volume: 58 start-page: 6911 year: 2019 ident: C9CC06260B-(cit14)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201900465 – volume: 26 start-page: 5429 year: 2014 ident: C9CC06260B-(cit17)/*[position()=1] publication-title: Adv. Mater. doi: 10.1002/adma.201401356 – volume: 115 start-page: 5014 year: 2015 ident: C9CC06260B-(cit11)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr5004425 – volume: 12 start-page: 244 year: 2015 ident: C9CC06260B-(cit3)/*[position()=1] publication-title: Nat. Methods doi: 10.1038/nmeth.3256 – volume: 91 start-page: 4172 year: 2019 ident: C9CC06260B-(cit32)/*[position()=1] publication-title: Anal. Chem. doi: 10.1021/acs.analchem.9b00224 – volume: 137 start-page: 6781 year: 2015 ident: C9CC06260B-(cit20)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.5b03548 – volume: 57 start-page: 3963 year: 2018 ident: C9CC06260B-(cit30)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201712949 – volume: 89 start-page: 11427 year: 2017 ident: C9CC06260B-(cit23)/*[position()=1] publication-title: Anal. Chem. doi: 10.1021/acs.analchem.7b02538 – volume: 140 start-page: 7716 year: 2018 ident: C9CC06260B-(cit6)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.8b04404 – volume: 54 start-page: 7332 year: 2015 ident: C9CC06260B-(cit21)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201502365 – volume: 149 start-page: 253 year: 2018 ident: C9CC06260B-(cit31)/*[position()=1] publication-title: Dyes Pigm. doi: 10.1016/j.dyepig.2017.10.002 – volume: 56 start-page: 12543 year: 2017 ident: C9CC06260B-(cit22)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201706517 – volume: 9 start-page: 855 year: 2014 ident: WOS:000334823200003 article-title: Bright Building Blocks for Chemical Biology publication-title: ACS CHEMICAL BIOLOGY doi: 10.1021/cb500078u – volume: 138 start-page: 6960 year: 2016 ident: WOS:000377643300014 article-title: Aziridinyl Fluorophores Demonstrate Bright Fluorescence and Superior Photostability by Effectively Inhibiting Twisted Intramolecular Charge Transfer publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.6b03924 – volume: 133 start-page: 6642 year: 2011 ident: WOS:000290363400031 article-title: Emission Wavelength Prediction of a Full-Color-Tunable Fluorescent Core Skeleton, 9-Aryl-1,2-dihydropyrrolo[3,4-b]indolizin-3-one publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja110766a – volume: 56 start-page: 7831 year: 2017 ident: WOS:000403839000024 article-title: Intermolecular Charge-Transfer Interactions Facilitate Two-Photon Absorption in Styrylpyridine-Tetracyanobenzene Cocrystals publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201703439 – volume: 137 start-page: 6781 year: 2015 ident: WOS:000355890600013 article-title: Two-Photon Absorbing Dyes with Minimal Autofluorescence in Tissue Imaging: Application to in Vivo Imaging of Amyloid-beta Plaques with a Negligible Background Signal publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.5b03548 – volume: 140 start-page: 7716 year: 2018 ident: WOS:000436211600053 article-title: A General Method To Increase Stokes Shift by Introducing Alternating Vibronic Structures publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.8b04404 – volume: 101 start-page: 1267 year: 2001 ident: WOS:000168684700008 article-title: Big is beautiful - "Aromaticity" revisited from the viewpoint of macromolecular and supramolecular benzene chemistry publication-title: CHEMICAL REVIEWS doi: 10.1021/cr990322p – volume: 57 start-page: 3963 year: 2018 ident: WOS:000428350200016 article-title: Cocrystals Strategy towards Materials for Near-Infrared Photothermal Conversion and Imaging publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201712949 – volume: 4 start-page: ARTN 2061 year: 2013 ident: WOS:000323668400004 article-title: Three-dimensional deep sub-diffraction optical beam lithography with 9 nm feature size publication-title: NATURE COMMUNICATIONS doi: 10.1038/ncomms3061 – volume: 100 start-page: 1973 year: 2000 ident: WOS:000087778100003 article-title: Cyanines during the 1990s: A review publication-title: CHEMICAL REVIEWS doi: 10.1021/cr990402t – volume: 56 start-page: 16611 year: 2017 ident: WOS:000418359400035 article-title: A General Strategy for Development of Near-Infrared Fluorescent Probes for Bioimaging publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201710688 – volume: 110 start-page: 2620 year: 2010 ident: WOS:000277811600003 article-title: New Strategies for Fluorescent Probe Design in Medical Diagnostic Imaging publication-title: CHEMICAL REVIEWS doi: 10.1021/cr900263j – volume: 7 start-page: ARTN x year: 2016 ident: WOS:000379086400001 article-title: Development of background-free tame fluorescent probes for intracellular live cell imaging publication-title: NATURE COMMUNICATIONS doi: 10.1038/ncomms11964 – volume: 54 start-page: 7332 year: 2015 ident: WOS:000356390300019 article-title: Single Benzene Green Fluorophore: Solid-State Emissive, Water-Soluble, and Solvent-and pH-Independent Fluorescence with Large Stokes Shifts publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201502365 – volume: 56 start-page: 12543 year: 2017 ident: WOS:000411810600020 article-title: Efficient Red-Emissive Organic Crystals with Amplified Spontaneous Emissions Based on a Single Benzene Framework publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201706517 – volume: 89 start-page: 11427 year: 2017 ident: WOS:000414887000040 article-title: Rational Engineering of Bioinspired Anthocyanidin Fluorophores with Excellent Two-Photon Properties for Sensing and Imaging publication-title: ANALYTICAL CHEMISTRY doi: 10.1021/acs.analchem.7b02538 – volume: 57 start-page: 7473 year: 2018 ident: WOS:000434949200034 article-title: Enhancing the Anti-Solvatochromic Two-Photon Fluorescence for Cirrhosis Imaging by Forming a Hydrogen-Bond Network publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201800293 – volume: 18 start-page: 28198 year: 2016 ident: WOS:000385180600056 article-title: Aggregates of quadrupolar dyes for two-photon absorption: the role of intermolecular interactions publication-title: PHYSICAL CHEMISTRY CHEMICAL PHYSICS doi: 10.1039/c6cp05153g – volume: 9 start-page: 6497 year: 2018 ident: WOS:000442262400005 article-title: Exploration of biocompatible AIEgens from natural resources publication-title: CHEMICAL SCIENCE doi: 10.1039/c8sc01635f – volume: 3 start-page: 142 year: 2008 ident: WOS:000254218800003 article-title: Bright ideas for chemical biology publication-title: ACS CHEMICAL BIOLOGY doi: 10.1021/cb700248m – volume: 149 start-page: 253 year: 2018 ident: WOS:000423246900028 article-title: Selective visualization of hypochlorite and its fluctuation in cancer cells by a mitochondria-targeting ratiometric fluorescent probe publication-title: DYES AND PIGMENTS doi: 10.1016/j.dyepig.2017.10.002 – volume: 398 start-page: 51 year: 1999 ident: WOS:000079033900047 article-title: Two-photon polymerization initiators for three-dimensional optical data storage and microfabrication publication-title: NATURE – volume: 26 start-page: 5429 year: 2014 ident: WOS:000340680700008 article-title: Aggregation-Induced Emission: The Whole Is More Brilliant than the Parts publication-title: ADVANCED MATERIALS doi: 10.1002/adma.201401356 – volume: 58 start-page: 6911 year: 2019 ident: WOS:000476423300011 article-title: SCOTfluors: Small, Conjugatable, Orthogonal, and Tunable Fluorophores for InVivo Imaging of Cell Metabolism publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201900465 – volume: 58 start-page: 8405 year: 2019 ident: WOS:000476608700019 article-title: Developing Through-Space Charge Transfer Polymers as a General Approach to Realize Full-Color and White Emission with Thermally Activated Delayed Fluorescence publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201902264 – volume: 115 start-page: 5014 year: 2015 ident: WOS:000356316300009 article-title: Small-Molecule Two-Photon Probes for Bioimaging Applications publication-title: CHEMICAL REVIEWS doi: 10.1021/cr5004425 – volume: 29 start-page: ARTN 1807623 year: 2019 ident: WOS:000473101200006 article-title: Near-Infrared (NIR) Organic Light-Emitting Diodes (OLEDs): Challenges and Opportunities publication-title: ADVANCED FUNCTIONAL MATERIALS doi: 10.1002/adfm.201807623 – volume: 40 start-page: 5361 year: 2011 ident: WOS:000295921500012 article-title: Aggregation-induced emission publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c1cs15113d – volume: 113 start-page: 15845 year: 2009 ident: WOS:000269654700012 article-title: Twisted Intramolecular Charge Transfer and Aggregation-Induced Emission of BODIPY Derivatives publication-title: JOURNAL OF PHYSICAL CHEMISTRY C doi: 10.1021/jp902962h – volume: 6 start-page: 4335 year: 2015 ident: WOS:000356176200085 article-title: A structural remedy toward bright dipolar fluorophores in aqueous media publication-title: CHEMICAL SCIENCE doi: 10.1039/c5sc01076d – volume: 91 start-page: 4172 year: 2019 ident: WOS:000462098300056 article-title: In Vivo Imaging of Endogenously Produced HClO in Zebrafish and Mice Using a Bright, Photostable Ratiometric Fluorescent Probe publication-title: ANALYTICAL CHEMISTRY doi: 10.1021/acs.analchem.9b00224 – volume: 12 start-page: 244 year: 2015 ident: WOS:000350670300026 article-title: A general method to improve fluorophores for live-cell and single-molecule microscopy publication-title: NATURE METHODS doi: 10.1038/NMETH.3256 |
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Snippet | We report here a single-benzene based fluorescent framework, amino-terephthalonitrile, denoted
SB-Fluor
. This scaffold displays versatile emission wavelength... We report here a single-benzene based fluorescent framework, amino-terephthalonitrile, denoted SB-Fluor. This scaffold displays versatile emission wavelength... |
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SubjectTerms | Benzene chemical reactions Chemistry Chemistry, Multidisciplinary Crystallography Emission Fluorescence fluorescent dyes Hydrocarbons Mechanoluminescence Physical Sciences Polymorphism Science & Technology Solid state wavelengths |
Title | A general strategy for development of a single benzene fluorophore with full-color-tunable, environmentally insensitive, and two-photon solid-state emission |
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