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Biblioteca

MARC Lista (tabellare)
Advances in photochemistry . Volume 13 [[electronic resource] /] / editors, David H. Volman, George S. Hammond, Klaus Gollnick
Advances in photochemistry . Volume 13 [[electronic resource] /] / editors, David H. Volman, George S. Hammond, Klaus Gollnick
Pubbl/distr/stampa New York, : Wiley-Interscience, 1968
Descrizione fisica 1 online resource (514 p.)
Disciplina 541.35
541.35082
Altri autori (Persone) VolmanDavid H
HammondGeorge S <1921-2005.> (George Simms)
GollnickKlaus
Collana Advances in photochemistry
Soggetto topico Photochemistry
Chemistry, Physical and theoretical
ISBN 1-282-30552-2
9786612305528
0-470-13343-0
0-470-13371-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Advances in Photochemistry; Contents; Photodissociation Dynamics of Small Molecules; Quantum Theory of Polyatomic Photodissociation; Bimolecular Photochemical Reactions of the Stilbenes; Photoinduced Electron Transfer in Organic Systems: Control of Back Electron Transfer; Chemical Sensitization, Spectral Sensitization, and Latent Image Formation in Silver Halide Photography; Dye Sensitized Photopolymerization; Index; Cumulative Index, Volumes 1-13
Record Nr. UNINA-9910829997803321
New York, : Wiley-Interscience, 1968
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Advances in photochemistry . Volume 13 [[electronic resource] /] / editors, David H. Volman, George S. Hammond, Klaus Gollnick
Advances in photochemistry . Volume 13 [[electronic resource] /] / editors, David H. Volman, George S. Hammond, Klaus Gollnick
Pubbl/distr/stampa New York, : Wiley-Interscience, 1968
Descrizione fisica 1 online resource (514 p.)
Disciplina 541.35
541.35082
Altri autori (Persone) VolmanDavid H
HammondGeorge S <1921-2005.> (George Simms)
GollnickKlaus
Collana Advances in photochemistry
Soggetto topico Photochemistry
Chemistry, Physical and theoretical
ISBN 1-282-30552-2
9786612305528
0-470-13343-0
0-470-13371-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Advances in Photochemistry; Contents; Photodissociation Dynamics of Small Molecules; Quantum Theory of Polyatomic Photodissociation; Bimolecular Photochemical Reactions of the Stilbenes; Photoinduced Electron Transfer in Organic Systems: Control of Back Electron Transfer; Chemical Sensitization, Spectral Sensitization, and Latent Image Formation in Silver Halide Photography; Dye Sensitized Photopolymerization; Index; Cumulative Index, Volumes 1-13
Record Nr. UNINA-9910841343103321
New York, : Wiley-Interscience, 1968
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Advances in photochemistry . Volume 5 [[electronic resource] /] / editors, W. Albert Noyes, Jr., George S. Hammond, J.N. Pitts, Jr
Advances in photochemistry . Volume 5 [[electronic resource] /] / editors, W. Albert Noyes, Jr., George S. Hammond, J.N. Pitts, Jr
Pubbl/distr/stampa New York, : Wiley-Interscience, 1968
Descrizione fisica 1 online resource (412 p.)
Disciplina 541.35
541.35082
Altri autori (Persone) NoyesW. Albert <1898-1980.> (William Albert)
HammondGeorge S <1921-2005.> (George Simms)
PittsJames N
Collana Advances in photochemistry
Soggetto topico Photochemistry
Chemistry, Physical and theoretical
ISBN 1-282-31446-7
9786612314469
0-470-13335-X
0-470-13362-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Advances in Photochemistry; Contents; The Spectra and Structures of Triatomic Free Radicals; Properties and Reactions of Organic Molecules in their Triplet State; The Role of Nitric Oxide in Photochemistry; lsomerization as a Route for Radiationless Transitions; Author Index; Subject Index; Cumulative Index
Record Nr. UNINA-9910840722503321
New York, : Wiley-Interscience, 1968
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Applications of lasers to chemical problems / Edited by Ted R. Evans
Applications of lasers to chemical problems / Edited by Ted R. Evans
Pubbl/distr/stampa New York : J. Wiley & Sons, copyr. 1982
Descrizione fisica XI, 291 p. : graf. tab. ; 21 cm
Disciplina 541.35
Collana Techniques of chemistry
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISA-990003282540203316
New York : J. Wiley & Sons, copyr. 1982
Materiale a stampa
Lo trovi qui: Univ. di Salerno
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Applied Photochemistry [[electronic resource] ] : When Light Meets Molecules / / edited by Giacomo Bergamini, Serena Silvi
Applied Photochemistry [[electronic resource] ] : When Light Meets Molecules / / edited by Giacomo Bergamini, Serena Silvi
Edizione [1st ed. 2016.]
Pubbl/distr/stampa Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016
Descrizione fisica 1 online resource (VI, 533 p. 485 illus., 193 illus. in color.)
Disciplina 541.35
Collana Lecture Notes in Chemistry
Soggetto topico Physical chemistry
Renewable energy resources
Medicine
Physical Chemistry
Renewable and Green Energy
Medicine/Public Health, general
ISBN 3-319-31671-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 1. Supramolecular Artificial Photosynthesis -- 2. Solar Energy Conversion in Photoelectrochemical Systems -- 3. Organic Light-Emitting Diodes (OLEDs): Working Principles and Device Technology -- 4. Light-Emitting Electrochemical Cells -- 5. Industrial Photochromism -- 6. Application of Visible and Solar Light in Organic Synthesis -- 7. Photochemical Reactions in Sunlit Surface Waters -- 8. Photodynamic Therapy -- 9. Polymer Nanoparticles for Cancer Photodynamic Therapy Combined with Nitric Oxide Photo release and Chemotherapy -- 10. Chemiluminescence in Biomedicine -- 11. Solar Filters: A Strategy of Photo protection -- 12. Luminescent Chemosensors: From Molecules to Nanostructures -- 13. Photochemistry for Cultural Heritage. .
Record Nr. UNINA-9910254034103321
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016
Materiale a stampa
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Applied Photochemistry [[electronic resource] /] / edited by Rachel C. Evans, Peter Douglas, Hugh D. Burrow
Applied Photochemistry [[electronic resource] /] / edited by Rachel C. Evans, Peter Douglas, Hugh D. Burrow
Edizione [1st ed. 2013.]
Pubbl/distr/stampa Dordrecht : , : Springer Netherlands : , : Imprint : Springer, , 2013
Descrizione fisica 1 online resource (619 p.)
Disciplina 541.35
Soggetto topico Physical chemistry
Environmental chemistry
Optical materials
Electronic materials
Medicine
Physical Chemistry
Environmental Chemistry
Optical and Electronic Materials
Biomedicine, general
ISBN 90-481-3830-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Foundations of Photochemistry: A Background on the Interaction Between Light and Molecules -- Photochemical Synthesis -- Inorganic Photochemistry -- Photochemical Materials: Absorbers, Emitters, Displays, Sensitisers, Acceptors, Traps and Photochromics -- Atmospheric Photochemistry -- Photodegradation of Pesticides and Photocatalysis in the Treatment of Water and Waste -- Solar Energy Conversion -- Radiolytic and Photolytic Production of Free Radicals and Reactive Oxygen Species: Interactions with Antioxidants and Biomolecules -- Photomedicine -- Photochemistry in Medical Diagnostics -- Photochemical Imaging -- Optical Sensors and Probes -- Photochemistry in Electronics -- The Photochemical Laboratory -- Experimental Techniques for Excited State Characterisation.
Record Nr. UNINA-9910437807503321
Dordrecht : , : Springer Netherlands : , : Imprint : Springer, , 2013
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Bioluminescence and chemiluminescence / edited by Marlene A. DeLuca
Bioluminescence and chemiluminescence / edited by Marlene A. DeLuca
Pubbl/distr/stampa New York, : Academic Press, 1978
Descrizione fisica XXI, 653 p. : ill. ; 24 cm
Disciplina 541.35
Collana Methods in Enzymology
Soggetto non controllato BIOLUMINESCENZA
CHEMILUMINESCENZA
ISBN 0121819574
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910646998203321
New York, : Academic Press, 1978
Materiale a stampa
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Die Chemilumineszenz Der 2-Coumaranone : Synthese, Lumineszenzmechanismus und Applikation / / Stefan Schramm
Die Chemilumineszenz Der 2-Coumaranone : Synthese, Lumineszenzmechanismus und Applikation / / Stefan Schramm
Autore Schramm Stefan
Pubbl/distr/stampa Berlin : , : Logos Verlag, , [2016]
Descrizione fisica 1 online resource (278 pages)
Disciplina 541.35
Soggetto topico Chemiluminescence
ISBN 3-8325-8816-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione ger
Record Nr. UNINA-9910793935903321
Schramm Stefan  
Berlin : , : Logos Verlag, , [2016]
Materiale a stampa
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Die Chemilumineszenz Der 2-Coumaranone : Synthese, Lumineszenzmechanismus und Applikation / / Stefan Schramm
Die Chemilumineszenz Der 2-Coumaranone : Synthese, Lumineszenzmechanismus und Applikation / / Stefan Schramm
Autore Schramm Stefan
Pubbl/distr/stampa Berlin : , : Logos Verlag, , [2016]
Descrizione fisica 1 online resource (278 pages)
Disciplina 541.35
Soggetto topico Chemiluminescence
ISBN 3-8325-8816-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione ger
Record Nr. UNINA-9910813601903321
Schramm Stefan  
Berlin : , : Logos Verlag, , [2016]
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Chiral Luminescence : From Molecules to Materials and Devices
Chiral Luminescence : From Molecules to Materials and Devices
Autore Akagi Kazuo
Edizione [1st ed.]
Pubbl/distr/stampa Newark : , : John Wiley & Sons, Incorporated, , 2024
Descrizione fisica 1 online resource (984 pages)
Disciplina 541.35
ISBN 3-527-84111-3
3-527-84109-1
3-527-84110-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover -- Title Page -- Copyright -- Contents -- Preface -- Acknowledgments -- Section I Molecules -- Chapter 1 Synthesis and Properties of Circularly Polarized Luminescence‐Active Molecules Based on the Binaphthyl Skeleton -- 1.1 Introduction -- 1.2 Synthesis and Properties of Carbon‐Chain‐Bridged BINOL Derivatives -- 1.2.1 Synthesis of Carbon‐Chain‐Bridged BINOL Derivatives 6‐PAn and 7‐PAn -- 1.2.2 Optical Properties of Carbon‐Chain‐Bridged BINOL Derivatives 6‐PAn and 7‐PAn -- 1.3 Synthesis and Properties of BINOL Derivatives with PA Groups at the 3,3′‐ to 7,7′‐positions of the BINOL Skeleton (3‐PA1 to 7‐PA1) -- 1.3.1 Synthesis of bis‐PA BINOL Derivatives -- 1.3.2 Optical Properties of 3‐PA1 to 7‐PA1 -- 1.4 Synthesis and Properties of BINOL Derivatives with Multiple PA Groups -- 1.4.1 Synthesis of 3,6‐PA1 -- 1.4.2 Synthesis of 5,6‐PA1 -- 1.4.3 Synthesis of 6,7‐PA1 -- 1.4.4 Synthesis of 3,4,6‐PA1 -- 1.4.5 Optical Properties of Tetra‐ and Hexa‐PA1 Compounds -- 1.5 Conclusions -- Acknowledgments -- References -- Chapter 2 An Approach for the Qualitative Understanding of Electronic and Magnetic Transition Moments Aiming at the Design of CPL Chromophore Having Enhanced Chiroptical Properties -- 2.1 Introduction -- 2.2 What are Electronic and Magnetic Transition Moments, μ and m? -- 2.2.1 A Basic Background -- 2.2.2 Electronic Transition Moment μ and Position Operator -- 2.2.3 Qualitative Understanding of Electronic Transition Moment -- 2.2.4 Nature of Angular Momentum Operator -- 2.2.5 Qualitative Understanding of Magnetic Transition Moment -- 2.3 Tutorial: Why Previous Researchers Used Carbonyl Compounds as the Model of CPL Chromophore? -- 2.4 Conclusion -- References -- Chapter 3 Optical Resolution and Chiroptical Properties of Partially‐Overlapped Carbazolophanes -- 3.1 Introduction -- 3.2 Synthesis and Structural Feature of Carbazolophanes.
3.2.1 Cyclophanes Including Carbazolophanes as Excimer Models -- 3.2.2 Synthesis of Carbazolophanes -- 3.2.3 Structural Feature of Carbazolophanes -- 3.3 Optical Resolution of Carbazolophanes -- 3.3.1 Introduction -- 3.3.2 Optical Resolution of Carbazolophanes by Chiral HPLC -- 3.3.3 Isolation of Optically Active Carbazolophanes -- 3.4 Photophysical and Chiroptical Properties of Carbazolophanes -- 3.4.1 Introduction -- 3.4.2 Photophysical Properties of Carbazolophanes -- 3.4.2.1 Electronic Absorption Spectra of [3.3]PO‐ and [3.3]FO‐Carbazolophanes -- 3.4.2.2 Fluorescence Spectra of [3.3]PO‐ and [3.3]FO‐Carbazolophanes -- 3.4.2.3 Electronic Absorption and Fluorescence Spectra of [3.n]PO‐Carbazolophanes -- 3.4.3 Chiroptical Properties of Carbazolophanes -- 3.4.3.1 Absolute Configuration and Circular Dichromism (CD) Spectra of Carbazolophanes -- 3.4.3.2 The glum Charts of Carbazolophanes -- 3.4.3.3 Correlation Between the Structure of Carbazolophane and |glum| -- 3.5 Concluding Remark -- References -- Chapter 4 Circularly Polarized Luminescence in Stereogenic π‐Conjugated Macrocycles -- 4.1 Introduction -- 4.2 Basic Concept of Molecular Design -- 4.3 Stereogenic Cyclic Oligoarene -- 4.4 Twisted Cycloparaphenylenes -- 4.5 Figure‐eight System -- 4.6 Chiral Macrocycles Composed of Acetylene Scaffold -- 4.7 Summary and Outlook -- References -- Chapter 5 Developments in Circularly Polarized Luminescence Research Employing Cyclodextrins -- 5.1 Introduction -- 5.2 CPL Induction of Achiral Luminophores in a Cyclodextrin Cavity -- 5.2.1 CPL from Fluorescein Encapsulated in β‐CyD -- 5.2.2 CPL from CyD Linked with a Dancyl Dye -- 5.2.3 CPL from Pyrene Excimer in γ‐CyD -- 5.2.4 CPL from Excimer Dye/γ‐CyD Rotaxanes -- 5.3 Isolated Cyclodextrin Molecules Exhibiting CPL -- 5.3.1 Bright CPL from Cyclodextrin with Multiple Pyrene Units.
5.4 CPL Exhibiting Supramolecular Assembly Consisting of Cyclodextrins -- 5.4.1 Cyclodextrin Supramolecular Assembly with CPL Property -- 5.4.2 Stimuli‐responsive CyD Supramolecular Assemblies with CPL Property -- 5.5 CPL Derived from Organic Frameworks Consisting of Cyclodextrins -- 5.5.1 CPL Induction by Cyclodextrin‐based Metal‐organic Framework (MOF) -- 5.5.2 CPL forms Two‐dimensional Chiral Polyrotaxane Monolayer -- 5.6 Conclusion -- References -- Chapter 6 Circularly Polarized Luminescence Based on Chiral AIEgens -- 6.1 Introduction -- 6.2 Molecular Structures of Chiral AIEgens -- 6.2.1 Silole and Cyanostilbene‐Cored Chiral AIEgens -- 6.2.2 TPE‐Cored Chiral AIEgens -- 6.2.3 Other Chiral AIEgens -- 6.2.4 Prochiral AIEgens -- 6.2.5 Chiral Induction Through Supramolecular AIEgen System -- 6.3 Circularly Polarized Luminescence Based on Chiral AIEgens -- 6.3.1 CPL from Silole and Cyanostilbene‐Cored AIEgens -- 6.3.2 CPL from TPE‐Cored AIEgens -- 6.3.3 CPL from Prochiral AIEgens and Chiral Transfer -- 6.3.4 CPOLEDs Based on Chiral AIEgens -- 6.4 Conclusions -- References -- Chapter 7 Planar Chiral [2.2]Paracyclophane: Excellent Circularly Polarized Luminescence Emitters -- 7.1 Introduction -- 7.2 Chiral π‐Stacked Molecules Based on Planar Chiral [2.2]paracyclophane -- 7.3 Chiral Cyclic Molecules Based on Planar Chiral [2.2]Paracyclophane -- 7.4 Control of Axial Chirality, Helicity, and Twisted Chirality by Planar Chirality of [2.2]Paracyclophane -- 7.5 Conclusion -- References -- Chapter 8 Nanometrical Helical Structures as Platform to Induce Chiroptical Properties to Achiral Components -- 8.1 Introduction -- 8.2 Molecular and Supramolecular Chirality from Gemini‐Tartrate Templates -- 8.2.1 Gemini‐tartrate Amphiphiles - Formation of Gels with Chiral Nanoribbon Structures -- 8.2.2 Organic-Inorganic Nanohelices.
8.2.3 Chirality of Siloxane Network of the Silica Nanohelices -- 8.3 Silica Nanohelices as Platforms to Organize Nonchiral Objects -- 8.3.1 Silica Helices as Platforms for Grafting Molecules -- 8.3.2 Silica Helices as Platforms for Grafting Nanoparticles -- 8.3.3 Coassembly of Chiral Self‐assembly and Achiral Dyes -- 8.4 Conclusion -- References -- Section II Oligomers and Polymers -- Chapter 9 Synthesis and Chiroptical Properties of Helically Stacked Conjugated Polymers -- 9.1 Introduction -- 9.2 CPL of Disubstituted Polyacetylenes with Lyotropic LC Behavior -- 9.2.1 Background of Disubstituted Polyacetylenes -- 9.2.2 LC behavior of di‐PAs -- 9.2.3 CD Properties of the di‐PAs -- 9.2.4 CPL Properties of the di‐PAs -- 9.2.5 Summary of the di‐PA Characteristics -- 9.3 Dynamic Switching and Amplification of CPL using Selective Reflection/Transmission of N*‐LCs -- 9.3.1 Selective Reflection/Transmission of N*‐LCs -- 9.3.2 Fabrication of CPL‐switchable Cells -- 9.3.3 Chiroptical Properties of the CPL‐Switchable Cell Systems -- 9.3.4 Summary of the CPL‐Switchable Cell Systems -- 9.4 Blue CPL of Spherulites with a Higher‐Order Helical Structure Consisting of Ionic Conjugated Polymers -- 9.4.1 Polymer Spherulites -- 9.4.2 Chiroptical Properties of the Assembled Cationic Conjugated Polymers -- 9.4.3 Interactions Between Cationic Conjugated Polymers and Anionic Chiral Compounds -- 9.4.4 Summary of the Polymer Spherulites -- 9.5 Conclusion -- References -- Chapter 10 Synthesis and Chiroptical Properties of Helical, Conjugated Polymers, and Twisted Molecules -- 10.1 Introduction -- 10.2 Polyurethane and Cyclic Oligomer -- 10.3 Polyfluorenes -- 10.4 Poly(fluorene‐2,7‐diylethene‐1,2‐diyl)s [poly(fluorenevinylene)s] -- 10.5 Poly(benzene‐1,4‐diyl)s [poly(p‐phenylene)s] -- 10.6 Chiral Small Molecules Having Twisted Conformation -- References.
Chapter 11 Chiroptical and Magneto‐optical Properties of Porphyrin Compounds -- 11.1 Exciton Chirality of Porphyrin Compounds -- 11.1.1 Electronic Absorption Spectra of Porphyrin Derivatives -- 11.1.2 Theoretical Background of Exciton Chirality -- 11.1.3 Application of Exciton Chirality to Porphyrin Dimers -- 11.1.4 Macroscopic Mechanical Rotation‐Induced Chirality of Porphyrin Aggregates -- 11.2 Magnetic Circular Dichroism of Porphyrin Compounds -- 11.2.1 Theoretical Background of Magnetic Circular Dichroism -- 11.2.2 Application of Magnetic Circular Dichroism to Porphyrin Compounds -- 11.2.2.1 Detection of Minor Tautomers -- 11.2.2.2 Observation of Singlet → Triplet Transitions -- 11.3 Magneto‐Chiral Dichroism of Porphyrin Aggregates -- 11.3.1 Theoretical Background of Magneto‐Chiral Dichroism -- 11.3.2 Magneto‐chiral Dichroism of Aromatic π‐Conjugated Systems -- 11.4 Circular Polarized and Magnetic Circular Luminescence of Porphyrin Aggregates -- 11.5 Harmonic Light of Chiral Porphyrin Aggregates -- References -- Chapter 12 CPL Emission from the Photo‐Excited Parallel‐Oriented Aryl/Aryl Dimer -- 12.1 Introduction -- 12.2 Background of this Chapter -- 12.2.1 Excimers -- 12.2.2 Circularly Polarized Light -- 12.2.3 Dissymmetry Factor -- 12.2.4 Rotatory Strength and Its AO‐level Decomposition -- 12.3 Examples of Parallelly Oriented Aryl/Aryl Dimer -- 12.3.1 Naphthalene Diimide as an Aryl Group -- 12.3.2 Naphthalene as an Aryl Group -- 12.4 Conclusion -- References -- Chapter 13 Synthesis, Control of Higher‐Order Structures, and Optical Properties of Platinum‐Containing Poly(aryleneethynylene)s and Related Compounds -- 13.1 Introduction -- 13.2 Synthesis of Pt‐containing Poly(aryleneethynylene)s by Sonogashira-Hagihara Coupling Polymerization -- 13.3 Synthesis of Pt‐containing Poly(aryleneethynylene)s by the Dehydrochlorination Coupling Polymerization.
13.4 Ligand Exchange Reaction for Controlling the Conformation of Pt‐containing Polymers.
Record Nr. UNINA-9910869199303321
Akagi Kazuo  
Newark : , : John Wiley & Sons, Incorporated, , 2024
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