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Volumn 28, Issue 21, 2016, Pages 7964-7972

Chameleonic, Light Harvesting Photonic Gels Based on Orthogonal Molecular Fibrillization

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOPHORES; ENERGY TRANSFER; FLUORESCENCE SPECTROSCOPY; GELS;

EID: 84994745691     PISSN: 08974756     EISSN: 15205002     Source Type: Journal    
DOI: 10.1021/acs.chemmater.6b03137     Document Type: Article
Times cited : (49)

References (70)
  • 1
    • 0001629673 scopus 로고    scopus 로고
    • Low Molecular Mass Gelators of Organic Liquids and the Properties of Their Gels
    • Terech, P.; Weiss, R. G. Low Molecular Mass Gelators of Organic Liquids and the Properties of Their Gels Chem. Rev. 1997, 97, 3133-3159 10.1021/cr9700282
    • (1997) Chem. Rev. , vol.97 , pp. 3133-3159
    • Terech, P.1    Weiss, R.G.2
  • 2
    • 84901700497 scopus 로고    scopus 로고
    • The Past, Present, and Future of Molecular Gels. What Is the Status of the Field, and Where Is It Going?
    • Weiss, R. G. The Past, Present, and Future of Molecular Gels. What Is the Status of the Field, and Where Is It Going? J. Am. Chem. Soc. 2014, 136, 7519-7530 10.1021/ja503363v
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 7519-7530
    • Weiss, R.G.1
  • 3
    • 54049115951 scopus 로고    scopus 로고
    • High-Tech Applications of Self-Assembling Supramolecular Nanostructured Gel-Phase Materials: From Regenerative Medicine to Electronic Devices
    • Hirst, A. R.; Escuder, B.; Miravet, J. F.; Smith, D. K. High-Tech Applications of Self-Assembling Supramolecular Nanostructured Gel-Phase Materials: From Regenerative Medicine to Electronic Devices Angew. Chem., Int. Ed. 2008, 47, 8002-8018 10.1002/anie.200800022
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 8002-8018
    • Hirst, A.R.1    Escuder, B.2    Miravet, J.F.3    Smith, D.K.4
  • 4
    • 70349386207 scopus 로고    scopus 로고
    • Supramolecular Gels 'in Action'
    • Banerjee, S.; Das, R. K.; Maitra, U. Supramolecular Gels 'in Action' J. Mater. Chem. 2009, 19, 6649-6687 10.1039/b819218a
    • (2009) J. Mater. Chem. , vol.19 , pp. 6649-6687
    • Banerjee, S.1    Das, R.K.2    Maitra, U.3
  • 5
    • 78751557975 scopus 로고    scopus 로고
    • Supramolecular Gel Chemistry: Developments over the Last Decade
    • Steed, J. W. Supramolecular Gel Chemistry: Developments over the Last Decade Chem. Commun. 2011, 47, 1379-1383 10.1039/C0CC03293J
    • (2011) Chem. Commun. , vol.47 , pp. 1379-1383
    • Steed, J.W.1
  • 6
    • 77953155679 scopus 로고    scopus 로고
    • Supramolecular Gels as Active Media for Organic Reactions and Catalysis
    • Escuder, B.; Rodriguez-Llansola, F.; Miravet, J. F. Supramolecular Gels as Active Media for Organic Reactions and Catalysis New J. Chem. 2010, 34, 1044-1054 10.1039/b9nj00764d
    • (2010) New J. Chem. , vol.34 , pp. 1044-1054
    • Escuder, B.1    Rodriguez-Llansola, F.2    Miravet, J.F.3
  • 7
    • 78649948844 scopus 로고    scopus 로고
    • What Kind of "soft Materials" Can We Design from Molecular Gels?
    • Dawn, A.; Shiraki, T.; Haraguchi, S.; Tamaru, S.-i.; Shinkai, S. What Kind of "Soft Materials" Can We Design from Molecular Gels? Chem.-Asian J. 2011, 6, 266-282 10.1002/asia.201000217
    • (2011) Chem. - Asian J. , vol.6 , pp. 266-282
    • Dawn, A.1    Shiraki, T.2    Haraguchi, S.3    Tamaru, S.-I.4    Shinkai, S.5
  • 9
    • 84925115312 scopus 로고    scopus 로고
    • Multicomponent Low Molecular Weight Gelators
    • Raeburn, J.; Adams, D. J. Multicomponent Low Molecular Weight Gelators Chem. Commun. 2015, 51, 5170-5180 10.1039/C4CC08626K
    • (2015) Chem. Commun. , vol.51 , pp. 5170-5180
    • Raeburn, J.1    Adams, D.J.2
  • 10
    • 84868155026 scopus 로고    scopus 로고
    • Supramolecular Gels Formed from Multi-Component Low Molecular Weight Species
    • Buerkle, L. E.; Rowan, S. J. Supramolecular Gels Formed from Multi-Component Low Molecular Weight Species Chem. Soc. Rev. 2012, 41, 6089-6102 10.1039/c2cs35106d
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 6089-6102
    • Buerkle, L.E.1    Rowan, S.J.2
  • 11
    • 58149240787 scopus 로고    scopus 로고
    • Controlled Self-Sorting in the Assembly of 'Multi-Gelator' Gels
    • Moffat, J. R.; Smith, D. K. Controlled Self-Sorting in the Assembly of 'Multi-Gelator' Gels Chem. Commun. 2009, 316-318 10.1039/B818058J
    • (2009) Chem. Commun. , pp. 316-318
    • Moffat, J.R.1    Smith, D.K.2
  • 12
    • 79955672698 scopus 로고    scopus 로고
    • Self-Sorting Multi-Gelator Gels-Mixing and Ageing Effects in Thermally Addressable Supramolecular Soft Nanomaterials
    • Smith, M. M.; Smith, D. K. Self-Sorting Multi-Gelator Gels-Mixing and Ageing Effects in Thermally Addressable Supramolecular Soft Nanomaterials Soft Matter 2011, 7, 4856-4860 10.1039/c1sm05316g
    • (2011) Soft Matter , vol.7 , pp. 4856-4860
    • Smith, M.M.1    Smith, D.K.2
  • 13
    • 79952858723 scopus 로고    scopus 로고
    • Spontaneous Orthogonal Self-Assembly of a Synergetic Gelator System
    • Garcia Velazquez, D.; Luque, R. Spontaneous Orthogonal Self-Assembly of a Synergetic Gelator System Chem.-Eur. J. 2011, 17, 3847-3849 10.1002/chem.201003014
    • (2011) Chem. - Eur. J. , vol.17 , pp. 3847-3849
    • Garcia Velazquez, D.1    Luque, R.2
  • 16
    • 84898654976 scopus 로고    scopus 로고
    • Insights into the Coassembly of Hydrogelators and Surfactants Based on Aromatic Peptide Amphiphiles
    • Fleming, S.; Debnath, S.; Frederix, P. W. J. M.; Hunt, N. T.; Ulijn, R. V. Insights into the Coassembly of Hydrogelators and Surfactants Based on Aromatic Peptide Amphiphiles Biomacromolecules 2014, 15, 1171-1184 10.1021/bm401720z
    • (2014) Biomacromolecules , vol.15 , pp. 1171-1184
    • Fleming, S.1    Debnath, S.2    Frederix, P.W.J.M.3    Hunt, N.T.4    Ulijn, R.V.5
  • 18
    • 41949112717 scopus 로고    scopus 로고
    • Preparation of Nanostructures by Orthogonal Self-Assembly of Hydrogelators and Surfactants
    • Brizard, A.; Stuart, M.; van Bommel, K.; Friggeri, A.; de Jong, M.; van Esch, J. Preparation of Nanostructures by Orthogonal Self-Assembly of Hydrogelators and Surfactants Angew. Chem., Int. Ed. 2008, 47, 2063-2066 10.1002/anie.200704609
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 2063-2066
    • Brizard, A.1    Stuart, M.2    Van Bommel, K.3    Friggeri, A.4    De Jong, M.5    Van Esch, J.6
  • 20
    • 84950326895 scopus 로고    scopus 로고
    • Photopatterned Multidomain Gels: Multi-Component Self-Assembled Hydrogels Based on Partially Self-Sorting 1,3:2,4-Dibenzylidene-D-Sorbitol Derivatives
    • Cornwell, D. J.; Daubney, O. J.; Smith, D. K. Photopatterned Multidomain Gels: Multi-Component Self-Assembled Hydrogels Based on Partially Self-Sorting 1,3:2,4-Dibenzylidene-D-Sorbitol Derivatives J. Am. Chem. Soc. 2015, 137, 15486-15492 10.1021/jacs.5b09691
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 15486-15492
    • Cornwell, D.J.1    Daubney, O.J.2    Smith, D.K.3
  • 22
    • 42149130269 scopus 로고    scopus 로고
    • Development of Bioinspired Artificial Photosynthetic Systems
    • Fukuzumi, S. Development of Bioinspired Artificial Photosynthetic Systems Phys. Chem. Chem. Phys. 2008, 10, 2283-2297 10.1039/b801198m
    • (2008) Phys. Chem. Chem. Phys. , vol.10 , pp. 2283-2297
    • Fukuzumi, S.1
  • 23
    • 84922932752 scopus 로고    scopus 로고
    • Photoinduced Charge and Energy Transfer in Molecular Wires
    • Gilbert, M.; Albinsson, B. Photoinduced Charge and Energy Transfer in Molecular Wires Chem. Soc. Rev. 2015, 44, 845-862 10.1039/C4CS00221K
    • (2015) Chem. Soc. Rev. , vol.44 , pp. 845-862
    • Gilbert, M.1    Albinsson, B.2
  • 24
    • 84938403312 scopus 로고    scopus 로고
    • Biological Applications of Supramolecular Assemblies Designed for Excitation Energy Transfer
    • Peng, H.-Q.; Niu, L.-Y.; Chen, Y.-Z.; Wu, L.-Z.; Tung, C.-H.; Yang, Q.-Z. Biological Applications of Supramolecular Assemblies Designed for Excitation Energy Transfer Chem. Rev. 2015, 115, 7502-7542 10.1021/cr5007057
    • (2015) Chem. Rev. , vol.115 , pp. 7502-7542
    • Peng, H.-Q.1    Niu, L.-Y.2    Chen, Y.-Z.3    Wu, L.-Z.4    Tung, C.-H.5    Yang, Q.-Z.6
  • 26
    • 73249138888 scopus 로고    scopus 로고
    • Synthesis of Conjugated Polymers for Organic Solar Cell Applications
    • Cheng, Y. J.; Yang, S. H.; Hsu, C. S. Synthesis of Conjugated Polymers for Organic Solar Cell Applications Chem. Rev. 2009, 109, 5868-5923 10.1021/cr900182s
    • (2009) Chem. Rev. , vol.109 , pp. 5868-5923
    • Cheng, Y.J.1    Yang, S.H.2    Hsu, C.S.3
  • 27
    • 83755172041 scopus 로고    scopus 로고
    • Peak External Photocurrent Quantum Efficiency Exceeding 100% Via Meg in a Quantum Dot Solar Cell
    • Semonin, O. E.; Luther, J. M.; Choi, S.; Chen, H.-Y.; Gao, J.; Nozik, A. J.; Beard, M. C. Peak External Photocurrent Quantum Efficiency Exceeding 100% Via Meg in a Quantum Dot Solar Cell Science 2011, 334, 1530-1533 10.1126/science.1209845
    • (2011) Science , vol.334 , pp. 1530-1533
    • Semonin, O.E.1    Luther, J.M.2    Choi, S.3    Chen, H.-Y.4    Gao, J.5    Nozik, A.J.6    Beard, M.C.7
  • 28
    • 84905263104 scopus 로고    scopus 로고
    • Energy Transfer in Supramolecular Materials for New Applications in Photonics and Electronics
    • Wong, K.-T.; Bassani, D. M. Energy Transfer in Supramolecular Materials for New Applications in Photonics and Electronics NPG Asia Mater. 2014, 6, e116 10.1038/am.2014.53
    • (2014) NPG Asia Mater. , vol.6 , pp. e116
    • Wong, K.-T.1    Bassani, D.M.2
  • 29
    • 84952325976 scopus 로고    scopus 로고
    • Bifunctional Polymer Nanocomposites as Hole-Transport Layers for Efficient Light Harvesting: Application to Perovskite Solar Cells
    • Wang, J.-Y.; Hsu, F.-C.; Huang, J.-Y.; Wang, L.; Chen, Y.-F. Bifunctional Polymer Nanocomposites as Hole-Transport Layers for Efficient Light Harvesting: Application to Perovskite Solar Cells ACS Appl. Mater. Interfaces 2015, 7, 27676-27684 10.1021/acsami.5b08157
    • (2015) ACS Appl. Mater. Interfaces , vol.7 , pp. 27676-27684
    • Wang, J.-Y.1    Hsu, F.-C.2    Huang, J.-Y.3    Wang, L.4    Chen, Y.-F.5
  • 30
    • 84942850234 scopus 로고    scopus 로고
    • Supramolecular Coordination Polymer Formed from Artificial Light-Harvesting Dendrimer
    • Lee, H.; Jeong, Y.-H.; Kim, J.-H.; Kim, I.; Lee, E.; Jang, W.-D. Supramolecular Coordination Polymer Formed from Artificial Light-Harvesting Dendrimer J. Am. Chem. Soc. 2015, 137, 12394-12399 10.1021/jacs.5b08092
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 12394-12399
    • Lee, H.1    Jeong, Y.-H.2    Kim, J.-H.3    Kim, I.4    Lee, E.5    Jang, W.-D.6
  • 31
    • 84936971433 scopus 로고    scopus 로고
    • Artificial Light-Harvesting Arrays for Solar Energy Conversion
    • Harriman, A. Artificial Light-Harvesting Arrays for Solar Energy Conversion Chem. Commun. 2015, 51, 11745-11756 10.1039/C5CC03577E
    • (2015) Chem. Commun. , vol.51 , pp. 11745-11756
    • Harriman, A.1
  • 32
    • 84897641325 scopus 로고    scopus 로고
    • Functional-Gelators and Their Applications
    • Babu, S. S.; Praveen, V. K.; Ajayaghosh, A. Functional-Gelators and Their Applications Chem. Rev. 2014, 114, 1973-2129 10.1021/cr400195e
    • (2014) Chem. Rev. , vol.114 , pp. 1973-2129
    • Babu, S.S.1    Praveen, V.K.2    Ajayaghosh, A.3
  • 36
  • 37
    • 34548782358 scopus 로고    scopus 로고
    • Pi-Organogels of Self-Assembled P-Phenylenevinylenes: Soft Materials with Distinct Size, Shape, and Functions
    • Ajayaghosh, A.; Praveen, V. K. Pi-Organogels of Self-Assembled P-Phenylenevinylenes: Soft Materials with Distinct Size, Shape, and Functions Acc. Chem. Res. 2007, 40, 644-656 10.1021/ar7000364
    • (2007) Acc. Chem. Res. , vol.40 , pp. 644-656
    • Ajayaghosh, A.1    Praveen, V.K.2
  • 38
    • 34548251814 scopus 로고    scopus 로고
    • Molecular Wire Encapsulated into Pi Organogels: Efficient Supramolecular Light-Harvesting Antennae with Color-Tunable Emission
    • Ajayaghosh, A.; Praveen, V. K.; Vijayakumar, C.; George, S. J. Molecular Wire Encapsulated into Pi Organogels: Efficient Supramolecular Light-Harvesting Antennae with Color-Tunable Emission Angew. Chem., Int. Ed. 2007, 46, 6260-6265 10.1002/anie.200701925
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 6260-6265
    • Ajayaghosh, A.1    Praveen, V.K.2    Vijayakumar, C.3    George, S.J.4
  • 39
    • 66249139936 scopus 로고    scopus 로고
    • Rgb Emission through Controlled Donor Self-Assemble and Modulation of Excitation Energy Transfer: A Novel Strategy to White-Light-Emitting Organogels
    • Vijayakumar, C.; Praveen, V. K.; Ajayaghosh, A. Rgb Emission through Controlled Donor Self-Assemble and Modulation of Excitation Energy Transfer: A Novel Strategy to White-Light-Emitting Organogels Adv. Mater. 2009, 21, 2059-2063 10.1002/adma.200802932
    • (2009) Adv. Mater. , vol.21 , pp. 2059-2063
    • Vijayakumar, C.1    Praveen, V.K.2    Ajayaghosh, A.3
  • 40
    • 84901626216 scopus 로고    scopus 로고
    • Oligo(Phenylenevinylene) Hybrids and Self-Assemblies: Versatile Materials for Excitation Energy Transfer
    • Praveen, V. K.; Ranjith, C.; Bandini, E.; Ajayaghosh, A.; Armaroli, N. Oligo(Phenylenevinylene) Hybrids and Self-Assemblies: Versatile Materials for Excitation Energy Transfer Chem. Soc. Rev. 2014, 43, 4222-4242 10.1039/c3cs60406c
    • (2014) Chem. Soc. Rev. , vol.43 , pp. 4222-4242
    • Praveen, V.K.1    Ranjith, C.2    Bandini, E.3    Ajayaghosh, A.4    Armaroli, N.5
  • 41
    • 33845650238 scopus 로고    scopus 로고
    • Self-Assembling and Light-Harvesting Properties of Fluorescent Linear Condensed Aromatic Gelators
    • Desvergne, J.-P.; Olive, A. G. L.; Sangeetha, N. M.; Reichwagen, J.; Hopf, H.; Del Guerzo, A. Self-Assembling and Light-Harvesting Properties of Fluorescent Linear Condensed Aromatic Gelators Pure Appl. Chem. 2006, 78, 2333-2339 10.1351/pac200678122333
    • (2006) Pure Appl. Chem. , vol.78 , pp. 2333-2339
    • Desvergne, J.-P.1    Olive, A.G.L.2    Sangeetha, N.M.3    Reichwagen, J.4    Hopf, H.5    Del Guerzo, A.6
  • 42
    • 29844456001 scopus 로고    scopus 로고
    • Energy Transfer in Self-Assembled N -Acene Fibers Involving ≥ 100 Donors per Acceptor
    • Del Guerzo, A.; Olive, A. G. L.; Reichwagen, J.; Hopf, H.; Desvergne, J. P. Energy Transfer in Self-Assembled N -Acene Fibers Involving ≥ 100 Donors Per Acceptor J. Am. Chem. Soc. 2005, 127, 17984-17985 10.1021/ja0566228
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 17984-17985
    • Del Guerzo, A.1    Olive, A.G.L.2    Reichwagen, J.3    Hopf, H.4    Desvergne, J.P.5
  • 44
    • 84922821806 scopus 로고    scopus 로고
    • Photon Upconversion in Supramolecular Gel Matrixes: Spontaneous Accumulation of Light-Harvesting Donor-Acceptor Arrays in Nanofibers and Acquired Air Stability
    • Duan, P.; Yanai, N.; Nagatomi, H.; Kimizuka, N. Photon Upconversion in Supramolecular Gel Matrixes: Spontaneous Accumulation of Light-Harvesting Donor-Acceptor Arrays in Nanofibers and Acquired Air Stability J. Am. Chem. Soc. 2015, 137, 1887-1894 10.1021/ja511061h
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 1887-1894
    • Duan, P.1    Yanai, N.2    Nagatomi, H.3    Kimizuka, N.4
  • 45
    • 39049094822 scopus 로고    scopus 로고
    • Tunable Red-Green-Blue Fluorescent Organogels on the Basis of Intermolecular Energy Transfer
    • Shu, T.; Wu, J.; Lu, M.; Chen, L.; Yi, T.; Li, F.; Huang, C. Tunable Red-Green-Blue Fluorescent Organogels on the Basis of Intermolecular Energy Transfer J. Mater. Chem. 2008, 18, 886-893 10.1039/b715462c
    • (2008) J. Mater. Chem. , vol.18 , pp. 886-893
    • Shu, T.1    Wu, J.2    Lu, M.3    Chen, L.4    Yi, T.5    Li, F.6    Huang, C.7
  • 46
    • 3242683774 scopus 로고    scopus 로고
    • Visible-Light-Harvesting Organogel Composed of Cholesterol-Based Perylene Derivatives
    • Sugiyasu, K.; Fujita, N.; Shinkai, S. Visible-Light-Harvesting Organogel Composed of Cholesterol-Based Perylene Derivatives Angew. Chem., Int. Ed. 2004, 43, 1229-1233 10.1002/anie.200352458
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 1229-1233
    • Sugiyasu, K.1    Fujita, N.2    Shinkai, S.3
  • 47
    • 84921688650 scopus 로고    scopus 로고
    • Energy Transfer within Responsive Pi-Conjugated Coassembled Peptide-Based Nanostructures in Aqueous Environments
    • Ardona, H. A. M.; Tovar, J. D. Energy Transfer within Responsive Pi-Conjugated Coassembled Peptide-Based Nanostructures in Aqueous Environments Chem. Sci. 2015, 6, 1474-1484 10.1039/C4SC03122A
    • (2015) Chem. Sci. , vol.6 , pp. 1474-1484
    • Ardona, H.A.M.1    Tovar, J.D.2
  • 48
    • 69849085466 scopus 로고    scopus 로고
    • Efficient Energy Transfer within Self-Assembling Peptide Fibers: A Route to Light-Harvesting Nanomaterials
    • Channon, K. J.; Devlin, G. L.; MacPhee, C. E. Efficient Energy Transfer within Self-Assembling Peptide Fibers: A Route to Light-Harvesting Nanomaterials J. Am. Chem. Soc. 2009, 131, 12520-12521 10.1021/ja902825j
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 12520-12521
    • Channon, K.J.1    Devlin, G.L.2    MacPhee, C.E.3
  • 49
    • 44349186044 scopus 로고    scopus 로고
    • Self-Sorting Organogels with P-N Heterojunction Points
    • Sugiyasu, K.; Kawano, S.-i.; Fujita, N.; Shinkai, S. Self-Sorting Organogels with P-N Heterojunction Points Chem. Mater. 2008, 20, 2863-2865 10.1021/cm800043b
    • (2008) Chem. Mater. , vol.20 , pp. 2863-2865
    • Sugiyasu, K.1    Kawano, S.-I.2    Fujita, N.3    Shinkai, S.4
  • 50
    • 4043080491 scopus 로고    scopus 로고
    • Synthesis of N-Type Perylene Bisimide Derivatives and Their Orthogonal Self-Assembly with P-Type Oligo(P-Phenylene Vinylene)S
    • van Herrikhuyzen, J.; Syamakumari, A.; Schenning, A.; Meijer, E. W. Synthesis of N-Type Perylene Bisimide Derivatives and Their Orthogonal Self-Assembly with P-Type Oligo(P-Phenylene Vinylene)S J. Am. Chem. Soc. 2004, 126, 10021-10027 10.1021/ja048819q
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 10021-10027
    • Van Herrikhuyzen, J.1    Syamakumari, A.2    Schenning, A.3    Meijer, E.W.4
  • 51
    • 84917710472 scopus 로고    scopus 로고
    • Nanofibers of Hydrogen-Bonded Two-Component Gel with Closely Connected P- and N-Channels and Photoinduced Electron Transfer
    • Xue, P.; Wang, P.; Yao, B.; Sun, J.; Gong, P.; Zhang, Z.; Qian, C.; Lu, R. Nanofibers of Hydrogen-Bonded Two-Component Gel with Closely Connected P- and N-Channels and Photoinduced Electron Transfer ACS Appl. Mater. Interfaces 2014, 6, 21426-21434 10.1021/am506422m
    • (2014) ACS Appl. Mater. Interfaces , vol.6 , pp. 21426-21434
    • Xue, P.1    Wang, P.2    Yao, B.3    Sun, J.4    Gong, P.5    Zhang, Z.6    Qian, C.7    Lu, R.8
  • 52
    • 84920837154 scopus 로고    scopus 로고
    • Organic Donor-Acceptor Assemblies Form Coaxial P-N Heterojunctions with High Photoconductivity
    • Prasanthkumar, S.; Ghosh, S.; Nair, V. C.; Saeki, A.; Seki, S.; Ajayaghosh, A. Organic Donor-Acceptor Assemblies Form Coaxial P-N Heterojunctions with High Photoconductivity Angew. Chem., Int. Ed. 2015, 54, 946-950 10.1002/anie.201408831
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 946-950
    • Prasanthkumar, S.1    Ghosh, S.2    Nair, V.C.3    Saeki, A.4    Seki, S.5    Ajayaghosh, A.6
  • 55
    • 79851493078 scopus 로고    scopus 로고
    • Interfacial Engineering of Organic Nanofibril Heterojunctions into Highly Photoconductive Materials
    • Che, Y.; Huang, H.; Xu, M.; Zhang, C.; Bunes, B. R.; Yang, X.; Zang, L. Interfacial Engineering of Organic Nanofibril Heterojunctions into Highly Photoconductive Materials J. Am. Chem. Soc. 2011, 133, 1087-1091 10.1021/ja109396g
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 1087-1091
    • Che, Y.1    Huang, H.2    Xu, M.3    Zhang, C.4    Bunes, B.R.5    Yang, X.6    Zang, L.7
  • 57
    • 78649304681 scopus 로고    scopus 로고
    • Colorimetric and Fluorescent Anion Sensors: An Overview of Recent Developments in the Use of 1,8-Naphthalimide-Based Chemosensors
    • Duke, R. M.; Veale, E. B.; Pfeffer, F. M.; Kruger, P. E.; Gunnlaugsson, T. Colorimetric and Fluorescent Anion Sensors: An Overview of Recent Developments in the Use of 1,8-Naphthalimide-Based Chemosensors Chem. Soc. Rev. 2010, 39, 3936-3953 10.1039/b910560n
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 3936-3953
    • Duke, R.M.1    Veale, E.B.2    Pfeffer, F.M.3    Kruger, P.E.4    Gunnlaugsson, T.5
  • 58
    • 84902094559 scopus 로고    scopus 로고
    • Recognition of Free Tryptophan in Water by Synthetic Pseudopeptides: Fluorescence and Thermodynamic Studies
    • Marti-Centelles, V.; Angeles Izquierdo, M.; Isabel Burguete, M.; Galindo, F.; Luis, S. V. Recognition of Free Tryptophan in Water by Synthetic Pseudopeptides: Fluorescence and Thermodynamic Studies Chem.-Eur. J. 2014, 20, 7465-7478 10.1002/chem.201304851
    • (2014) Chem. - Eur. J. , vol.20 , pp. 7465-7478
    • Marti-Centelles, V.1    Angeles Izquierdo, M.2    Isabel Burguete, M.3    Galindo, F.4    Luis, S.V.5
  • 59
    • 84935354375 scopus 로고
    • Experimentelle und Theoretische Untersuchung des Zwischenmolekularen Ubergangs von Elektronenanregungsenergie
    • Forster, T. Experimentelle Und Theoretische Untersuchung Des Zwischenmolekularen Ubergangs Von Elektronenanregungsenergie Zeitschrift Fur Naturforschung Section a-a Journal of Physical Sciences 1949, 4, 321-327
    • (1949) Zeitschrift fur Naturforschung Section A-a Journal of Physical Sciences , vol.4 , pp. 321-327
    • Forster, T.1
  • 61
    • 84880290938 scopus 로고    scopus 로고
    • Fret-Based Small-Molecule Fluorescent Probes: Rational Design and Bioimaging Applications
    • Yuan, L.; Lin, W.; Zheng, K.; Zhu, S. Fret-Based Small-Molecule Fluorescent Probes: Rational Design and Bioimaging Applications Acc. Chem. Res. 2013, 46, 1462-1473 10.1021/ar300273v
    • (2013) Acc. Chem. Res. , vol.46 , pp. 1462-1473
    • Yuan, L.1    Lin, W.2    Zheng, K.3    Zhu, S.4
  • 62
    • 84936883217 scopus 로고    scopus 로고
    • The Synthesis of New Fluorescent Bichromophoric Compounds as Ratiometric Ph Probes for Intracellular Measurements
    • Saura, A. V.; Marin, M. J.; Burguete, M. I.; Russell, D. A.; Galindo, F.; Luis, S. V. The Synthesis of New Fluorescent Bichromophoric Compounds as Ratiometric Ph Probes for Intracellular Measurements Org. Biomol. Chem. 2015, 13, 7736-7749 10.1039/C5OB00704F
    • (2015) Org. Biomol. Chem. , vol.13 , pp. 7736-7749
    • Saura, A.V.1    Marin, M.J.2    Burguete, M.I.3    Russell, D.A.4    Galindo, F.5    Luis, S.V.6
  • 63
    • 0031270032 scopus 로고    scopus 로고
    • Excellent Gelators for Organic Fluids: Simple Bolaform Amides Derived from Amino Acids
    • Hanabusa, K.; Tanaka, R.; Suzuki, M.; Kimura, M.; Shirai, H. Excellent Gelators for Organic Fluids: Simple Bolaform Amides Derived from Amino Acids Adv. Mater. 1997, 9, 1095-1097 10.1002/adma.19970091405
    • (1997) Adv. Mater. , vol.9 , pp. 1095-1097
    • Hanabusa, K.1    Tanaka, R.2    Suzuki, M.3    Kimura, M.4    Shirai, H.5
  • 64
    • 23144431706 scopus 로고    scopus 로고
    • Organogel Formation by Coaggregation of Adaptable Amidocarbamates and Their Tetraamide Analogues
    • Escuder, B.; Martí, S.; Miravet, J. F. Organogel Formation by Coaggregation of Adaptable Amidocarbamates and Their Tetraamide Analogues Langmuir 2005, 21, 6776-6787 10.1021/la050655j
    • (2005) Langmuir , vol.21 , pp. 6776-6787
    • Escuder, B.1    Martí, S.2    Miravet, J.F.3
  • 66
    • 13244273568 scopus 로고    scopus 로고
    • Extension of the Self-Consistent Spectrophotometric Basicity Scale in Acetonitrile to a Full Span of 28 Pka Units: Unification of Different Basicity Scales
    • Kaljurand, I.; Kütt, A.; Sooväli, L.; Rodima, T.; Mäemets, V.; Leito, I.; Koppel, I. A. Extension of the Self-Consistent Spectrophotometric Basicity Scale in Acetonitrile to a Full Span of 28 Pka Units: Unification of Different Basicity Scales J. Org. Chem. 2005, 70, 1019-1028 10.1021/jo048252w
    • (2005) J. Org. Chem. , vol.70 , pp. 1019-1028
    • Kaljurand, I.1    Kütt, A.2    Sooväli, L.3    Rodima, T.4    Mäemets, V.5    Leito, I.6    Koppel, I.A.7
  • 67
    • 33645506119 scopus 로고    scopus 로고
    • A Comprehensive Self-Consistent Spectrophotometric Acidity Scale of Neutral Brønsted Acids in Acetonitrile
    • Kütt, A.; Leito, I.; Kaljurand, I.; Sooväli, L.; Vlasov, V. M.; Yagupolskii, L. M.; Koppel, I. A. A Comprehensive Self-Consistent Spectrophotometric Acidity Scale of Neutral Brønsted Acids in Acetonitrile J. Org. Chem. 2006, 71, 2829-2838 10.1021/jo060031y
    • (2006) J. Org. Chem. , vol.71 , pp. 2829-2838
    • Kütt, A.1    Leito, I.2    Kaljurand, I.3    Sooväli, L.4    Vlasov, V.M.5    Yagupolskii, L.M.6    Koppel, I.A.7
  • 69
    • 67649850983 scopus 로고    scopus 로고
    • Unexpected Fluorescent Behavior of a 4-Amino-1,8-Naphthalimide Derived B-Cyclodextrin: Conformation Analysis and Sensing Properties
    • Zhong, C.; Mu, T.; Wang, L.; Fu, E.; Qin, J. Unexpected Fluorescent Behavior of a 4-Amino-1,8-Naphthalimide Derived B-Cyclodextrin: Conformation Analysis and Sensing Properties Chem. Commun. 2009, 4091-4093 10.1039/b902132a
    • (2009) Chem. Commun. , pp. 4091-4093
    • Zhong, C.1    Mu, T.2    Wang, L.3    Fu, E.4    Qin, J.5
  • 70
    • 84946935065 scopus 로고    scopus 로고
    • Aggregation-Induced Emission: Together We Shine, United We Soar!
    • Mei, J.; Leung, N. L. C.; Kwok, R. T. K.; Lam, J. W. Y.; Tang, B. Z. Aggregation-Induced Emission: Together We Shine, United We Soar! Chem. Rev. 2015, 115, 11718-11940 10.1021/acs.chemrev.5b00263
    • (2015) Chem. Rev. , vol.115 , pp. 11718-11940
    • Mei, J.1    Leung, N.L.C.2    Kwok, R.T.K.3    Lam, J.W.Y.4    Tang, B.Z.5


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