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Diels−Alder “Click Chemistry” for Highly Efficient Electrooptic Polymers
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Click Chemistry: Diverse Chemical Function from a Few Good Reactions
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Nanostructured Molecular Materials for Device-Quality, Highly Efficient Electrooptic Poled Polymers
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Organic Reversible Switching Devices for Memory Applications
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Polymer-Based Optical Waveguides: Materials, Processing, and Devices
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Design, Synthesis, and Properties of Highly Efficient Side-Chain Dendronized Nonlinear Optical Polymers for Electro-Optics
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Highly Efficient and Thermally Stable Electro‐optic Polymer from a Smartly Controlled Crosslinking Process
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Chemistry and Biology of Biosynthetic Diels–Alder Reactions
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Efficiency and Fidelity in a Click‐Chemistry Route to Triazole Dendrimers by the Copper( I )‐Catalyzed Ligation of Azides and Alkynes
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Towards Organo‐Click Chemistry: Development of Organocatalytic Multicomponent Reactions Through Combinations of Aldol, Wittig, Knoevenagel, Michael, Diels–Alder and Huisgen Cycloaddition Reactions
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Nonlinear Optical Polymeric Materials: From Chromophore Design to Commercial Applications
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Polymeric Materials and their Orientation Techniques for Second-Order Nonlinear Optics
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Dendrimers Clicked Together Divergently
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Click Chemistry: Versatility and Control in the Hands of Materials Scientists
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Facile preparation of poly(N-isopropylacrylamide)-based hydrogels via aqueous Diels–Alder click reaction
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A comprehensive investigation of the interrelationships between spectroscopy and photochemistry and substituents of some azulenic derivatives
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Energy-level modulation of organic alkynes by click chemistry
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Intrinsic friction analysis—Novel nanoscopic access to molecular mobility in constrained organic systems
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Electrically poled organic materials and thermo-optic materials
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01120openalex-snapshot
4,5,5-Trimethyl-2,5-dihydrofuran-Based Electron-Withdrawing Groups for NIR-Emitting Push–Pull Dipolar Fluorophores
inferred← citeshttps://doi.org/10.1021/acs.macromol.6b00721openalex-snapshot
Poly(bromoethyl acrylate): A Reactive Precursor for the Synthesis of Functional RAFT Materials
inferred← citeshttps://doi.org/10.1021/acs.macromol.8b01967openalex-snapshot
Unraveling Polymer Structures with RAFT Polymerization and Diels–Alder Chemistry
inferred← citeshttps://doi.org/10.1021/am800255topenalex-snapshot
Dendronlike Main-Chain Nonlinear Optical (NLO) Polyurethanes Constructed from “H”-Type Chromophores: Synthesis and NLO Properties
inferred← citeshttps://doi.org/10.1021/am900124copenalex-snapshot
“Click Chemistry” in Tailor-Made Polymethacrylates Bearing Reactive Furfuryl Functionality: A New Class of Self-Healing Polymeric Material
inferred← citeshttps://doi.org/10.1021/am900319hopenalex-snapshot
Synthesis and Nonlinear Optical Properties of a Peripherally Functionalized Hyperbranched Polymer by DR1 Chromophores
inferred← citeshttps://doi.org/10.1021/bk-2013-1144.ch025openalex-snapshot
Lignin-Based Graft CopolymersviaATRP and Click Chemistry
inferred← citeshttps://doi.org/10.1021/cm203590topenalex-snapshot
New Cross-Linkable Polymers with Huisgen Reaction Incorporating High μβ Chromophores for Second-Order Nonlinear Optical Applications
inferred← citeshttps://doi.org/10.1021/cr9000429openalex-snapshot
Electric Field Poled Organic Electro-optic Materials: State of the Art and Future Prospects
inferred← citeshttps://doi.org/10.1021/cr900157qopenalex-snapshot
Dendron-Mediated Self-Assembly, Disassembly, and Self-Organization of Complex Systems
inferred← citeshttps://doi.org/10.1021/ja8061612openalex-snapshot
Click-Type Reaction of Aromatic Polyamines for Improvement of Thermal and Optoelectronic Properties
inferred← citeshttps://doi.org/10.1021/jp066489lopenalex-snapshot
From Controllable Attached Isolation Moieties to Possibly Highly Efficient Nonlinear Optical Main-Chain Polyurethanes Containing Indole-Based Chromophores
inferred← citeshttps://doi.org/10.1021/jp7105988openalex-snapshot
New Indole-Based Chromophore-Containing Main-Chain Polyurethanes: Architectural Modification of Isolation Group, Enhanced Nonlinear Optical Property, and Improved Optical Transparency
inferred← citeshttps://doi.org/10.1021/jp712037jopenalex-snapshot
Binary Chromophore Systems in Nonlinear Optical Dendrimers and Polymers for Large Electrooptic Activities
inferred← citeshttps://doi.org/10.1021/jp907135fopenalex-snapshot
Two Types of Nonlinear Optical Polyurethanes Containing the Same Isolation Groups: Syntheses, Optical Properties, and Influence of Binding Mode
inferred← citeshttps://doi.org/10.1021/ma060690copenalex-snapshot
Anthracene−Maleimide-Based Diels−Alder “Click Chemistry” as a Novel Route to Graft Copolymers
inferred← citeshttps://doi.org/10.1021/ma061854sopenalex-snapshot
An Attempt To Modify Nonlinear Optical Effects of Polyurethanes by Adjusting the Structure of the Chromophore Moieties at the Molecular Level Using “Click” Chemistry
inferred← citeshttps://doi.org/10.1021/ma801875wopenalex-snapshot
Facile Attachment of Nonlinear Optical Chromophores to Polycarbonates
inferred← citeshttps://doi.org/10.1021/ma8025223openalex-snapshot
New Azo-Chromophore-Containing Hyperbranched Polytriazoles Derived from AB2 Monomers via Click Chemistry under Copper(I) Catalysis
inferred← citeshttps://doi.org/10.1021/ma802567xopenalex-snapshot
Molecular Design and Synthesis of Hetero-trichromophore for Enhanced Nonlinear Optical Activity
inferred← citeshttps://doi.org/10.1021/ma802612gopenalex-snapshot
Controlled Diels−Alder Reactions Used To Incorporate Highly Efficient Polyenic Chromophores into Maleimide-Containing Side-Chain Polymers for Electro-Optics
inferred← citeshttps://doi.org/10.1021/ma900471topenalex-snapshot
Nonlinear Optical Dendrimers from Click Chemistry: Convenient Synthesis, New Function of the Formed Triazole Rings, and Enhanced NLO Effects
inferred← citeshttps://doi.org/10.1021/mz200137mopenalex-snapshot
Model Diels–Alder Studies for the Creation of Amphiphilic Cross-Linked Networks as Healable, Antibiofouling Coatings
inferred← citeshttps://doi.org/10.1039/9781839169885-00024openalex-snapshot
Azide–Alkyne Click Chemistry and Multifunctional Polymers
inferred← citeshttps://doi.org/10.1039/9781839169885-00248openalex-snapshot
‘Click’ Chemistry in Polyurethanes: From Design to Applications
inferred← citeshttps://doi.org/10.1039/b718180aopenalex-snapshot
An atom-efficient conjugation approach to well-defined block copolymers using RAFT chemistry and hetero Diels–Alder cycloaddition
inferred← citeshttps://doi.org/10.1039/b901978mopenalex-snapshot
Marrying click chemistry with polymerization: expanding the scope of polymeric materials
inferred← citeshttps://doi.org/10.1039/b907173copenalex-snapshot
Rational molecular design and supramolecular assembly of highly efficient organic electro-optic materials
inferred← citeshttps://doi.org/10.1039/c0cs00205dopenalex-snapshot
Adapting semiconducting polymer doping techniques to create new types of click postfunctionalization
inferred← citeshttps://doi.org/10.1039/c1jm14254bopenalex-snapshot
Achieving excellent electro-optic activity and thermal stability in poled polymers through an expeditious crosslinking process
inferred← citeshttps://doi.org/10.1039/c1py00041aopenalex-snapshot
Diels–Alder “click” reactions: recent applications in polymer and material science
inferred← citeshttps://doi.org/10.1039/c2jm14591jopenalex-snapshot
A Diels–Alder crosslinkable host polymer for improved PLED performance: the impact on solution processed doped device and multilayer device performance
inferred← citeshttps://doi.org/10.1039/c5py01158bopenalex-snapshot
The utilization of post-synthetic modification in opto-electronic polymers: an effective complementary approach but not a competitive one to the traditional direct polymerization process
inferred← citeshttps://doi.org/10.1039/c7cc02980bopenalex-snapshot
A healable thermo-reversible functional polymer prepared via RAFT polymerization and ultrafast ‘click’ chemistry using a triazolinedione derivative
inferred← citeshttps://doi.org/10.1039/c9ra10813kopenalex-snapshot
Construction of a simple crosslinking system and its influence on the poling efficiency and oriental stability of organic electro-optic materials
inferred← citeshttps://doi.org/10.1039/d2qm00803copenalex-snapshot
Thermally crosslinkable second-order nonlinear optical polymer networks: high stability, good transparency, and large second-order nonlinear optical effects
inferred← citeshttps://doi.org/10.1080/15421400802329590openalex-snapshot
Thermally Stable Nonlinear Optical Polymers Based on Polyimides Substituted with Chromophores Containing Julolidine Moiety
inferred← citeshttps://doi.org/10.1117/12.864232openalex-snapshot
Copper(I)-catalyzed azide-alkyne cycloaddition for the synthesis of nonlinear electro-optic side-chain copolymers
inferred← citeshttps://doi.org/10.1186/s43074-021-00036-yopenalex-snapshot
Recent progress in electro-optic polymer for ultra-fast communication
inferred← citeshttps://doi.org/10.2478/s11696-014-0574-2openalex-snapshot
Click synthesis by Diels-Alder reaction and characterisation of hydroxypropyl methylcellulose-based hydrogels
inferred← citeshttps://doi.org/10.24820/ark.5550190.p011.623openalex-snapshot
Synthesis, analysis and study of sulfide-linked high functionality resin beads
inferred← citeshttps://doi.org/10.3390/polym12051084openalex-snapshot
The Use of Click-Type Reactions in the Preparation of Thermosets
inferred← citeshttps://doi.org/10.5012/bkcs.2010.31.12.3866openalex-snapshot
Synthesis and Nonlinear Optical Properties of Novel Polyester with Enhanced Second Harmonic Generation Thermal Stability
inferred← citeshttps://doi.org/10.5012/bkcs.2010.31.6.1509openalex-snapshot
Synthesis of Novel Y-type Nonlinear Optical Polyester with Enhanced Thermal Stability of Second Harmonic Generation for Electro-Optic Applications
inferred← citeshttps://doi.org/10.5012/bkcs.2011.32.9.3361openalex-snapshot
Synthesis and Properties of Novel Y-type Nonlinear Optical Polyester Containing Dioxynitroazobenzene Group with Enhanced Thermal Stability of Dipole Alignment
inferred← citeshttps://doi.org/10.5012/bkcs.2012.33.2.695openalex-snapshot
Synthesis and Properties of Novel Polyurethane Containing Nitrophenylazocatecholic Group as NLO Chromophore
inferred← citeshttps://doi.org/10.5012/bkcs.2012.33.4.1321openalex-snapshot
Synthesis and Nonlinear Optical Properties of Novel Y-type Polyimide Containing Dioxynitroazobenzene Group
inferred← citeshttps://doi.org/10.70675/ab759ae1zac1az4208z8b27z74c69a6c3856openalex-snapshot
Synthèse de réseaux polymères thermoréversibles par réaction de Diels-Alder
inferred← citeshttps://doi.org/10.70675/e8365007z9a6fz4ddfza74bz49274ad8cb72openalex-snapshot
Synthèse et caractérisations de réseaux thermosensibles à base époxy / amine par réactions de Diels-Alder
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