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Arylaminomaleimides as a New Class of Aggregation-induced Emission-active Molecules Obtained from Organoarsenic Compounds
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Reaction of Ambident Dianions with Oxalic Acid Dielectrophiles – Effect of the Heteroatoms of the Dinucleophile on the Regiochemistry of Cyclization
inferredcites →https://doi.org/10.1002/adfm.200801278openalex-snapshot
Functionalized Siloles: Versatile Synthesis, Aggregation‐Induced Emission, and Sensory and Device Applications
inferredcites →https://doi.org/10.1002/jhet.5570250634openalex-snapshot
Synthesis of 2,3‐quinolinedicarboxylic acid
inferredcites →https://doi.org/10.1002/pola.24792openalex-snapshot
Synthesis and fluorescent properties of model compounds for conjugated polymer containing maleimide units at the main chain
inferredcites →https://doi.org/10.1007/s10593-007-0134-6openalex-snapshot
Synthesis of 1-alkyl-3-arylamino-pyrrole-2,5-diones
inferredcites →https://doi.org/10.1007/s10593-008-0071-zopenalex-snapshot
2-Aminopyrrole-2,5-diones 2. Vinyl nucleophilic substitution of the alkylamino group in 1-alkyl-3-alkylaminopyrrole-2,5-diones by arylamines
inferredcites →https://doi.org/10.1007/s10895-010-0660-yopenalex-snapshot
Fluorescent Triphenyl Substituted Maleimide Derivatives: Synthesis, Spectroscopy and Quantum Chemical Calculations
inferredcites →https://doi.org/10.1016/j.cplett.2007.08.030openalex-snapshot
Endowing hexaphenylsilole with chemical sensory and biological probing properties by attaching amino pendants to the silolyl core
inferredcites →https://doi.org/10.1016/j.tet.2004.11.031openalex-snapshot
Arsonium ylides in organic synthesis
inferredcites →https://doi.org/10.1021/cm0303890openalex-snapshot
Bisindolylmaleimides as Red Electroluminescence Materials
inferredcites →https://doi.org/10.1021/cm2003269openalex-snapshot
Tuning the Electronic Nature of Aggregation-Induced Emission Luminogens with Enhanced Hole-Transporting Property
inferredcites →https://doi.org/10.1021/cr0306788openalex-snapshot
Hydroamination: Direct Addition of Amines to Alkenes and Alkynes
inferredcites →https://doi.org/10.1021/ja005875sopenalex-snapshot
Catalytic Solvent-Free Arsination: First Catalytic Application of Pd−Ar/As−Ph Exchange in the Syntheses of Functionalized Aryl Arsines
inferredcites →https://doi.org/10.1021/ja982657eopenalex-snapshot
Gas-Phase Basicity and Acidity Trends in α,β-Unsaturated Amines, Phosphines, and Arsines
inferredcites →https://doi.org/10.1021/jo00834a061openalex-snapshot
Maleimide syntheses by amine reaction with acetylenedicarboxylate esters
inferredcites →https://doi.org/10.1021/jo00892a008openalex-snapshot
Acetylenedicarbonyl fluoride. II. Its reaction with arylamines to yield isomaleimides, maleimides, and .alpha.-phenylimino- and .alpha.-phenylaminofuramides
inferredcites →https://doi.org/10.1021/jo101999bopenalex-snapshot
Multicolor Tuning of Aggregation-Induced Emission through Substituent Variation of Diphenyl-o-carborane
inferredcites →https://doi.org/10.1021/jp205525sopenalex-snapshot
Synthesis and Properties of Aggregation-Induced Emission Compounds Containing Triphenylethene and Tetraphenylethene Moieties
inferredcites →https://doi.org/10.1021/om070080gopenalex-snapshot
1,4-Dihydro-1,4-diarsinine: Facile Synthesis via Nonvolatile Arsenic Intermediates by Radical Reactions
inferredcites →https://doi.org/10.1021/om900727copenalex-snapshot
Synthesis and Characterization of Stereoisomers of 1,4-Dihydro-1,4-diarsinines
inferredcites →https://doi.org/10.1023/b:jocc.0000044091.78129.37openalex-snapshot
Unexpected chlorine substitution by hydrogen in the reaction of 2-chloro-3-p-toluidino-N-p-tolylmaleimide with DBU: Synthesis and molecular structure of 2-p-toluidino-N-p-tolylmaleimide
inferredcites →https://doi.org/10.1038/pj.2010.148openalex-snapshot
Synthesis and low-temperature dehydrating imidation polymerization of 1,4-dihydro-1,4-diarsininetetracarboxylic acid dianhydride
inferredcites →https://doi.org/10.1039/b105159hopenalex-snapshot
Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole
inferredcites →https://doi.org/10.1039/b111599eopenalex-snapshot
Strong fluorescence enhancement of 2-bromo-3-(1H-indol-3-yl)maleimide upon coordination to a Lewis-acidic metal complex
inferredcites →https://doi.org/10.1039/b211537aopenalex-snapshot
The colourful fluorescence from readily-synthesised 3,4-diaryl-substituted maleimide fluorophores
inferredcites →https://doi.org/10.1039/b904665hopenalex-snapshot
Aggregation-induced emission: phenomenon, mechanism and applications
inferredcites →https://doi.org/10.1039/c0cc03407jopenalex-snapshot
A new class of rhodamine luminophores: design, syntheses and aggregation-induced emission enhancement
inferredcites →https://doi.org/10.1039/c1cc14122hopenalex-snapshot
Towards high efficiency solid emitters with aggregation-induced emission and electron-transport characteristics
inferredcites →https://doi.org/10.1039/c1cc14642dopenalex-snapshot
New thermally stable aggregation-induced emission enhancement compounds for non-doped red organic light-emitting diodes
inferredcites →https://doi.org/10.1039/c1jm12098kopenalex-snapshot
A ratiometric fluorescent pH probe based on aggregation-induced emission enhancement and its application in live-cell imaging
inferredcites →https://doi.org/10.1039/c1jm14054jopenalex-snapshot
New tetraphenylethene-based efficient blue luminophors: aggregation induced emission and partially controllable emitting color
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Novel Thiomaleimide-Based Fluorescent Probe with Aggregation-Induced Emission for Detecting H2s
inferred← citeshttps://doi.org/10.2139/ssrn.4882723openalex-extracted
Novel Thiomaleimide-Based Fluorescent Probe with Aggregation-Induced Emission for Detecting H2s
inferred← citeshttps://doi.org/10.1002/adma.201401356openalex-snapshot
Aggregation‐Induced Emission: The Whole Is More Brilliant than the Parts
inferred← citeshttps://doi.org/10.1002/advs.202004299openalex-snapshot
Clusteroluminescence from Cluster Excitons in Small Heterocyclics Free of Aromatic Rings
inferred← citeshttps://doi.org/10.1002/ange.202410550openalex-snapshot
Substituted Maleimides: Self‐Reportable Linkers and Tags in Bioconjugation, Materials Science, and Nanotechnology
inferred← citeshttps://doi.org/10.1002/asia.201500499openalex-snapshot
A Mechanochromic Luminescent Dye Exhibiting On/Off Switching by Crystalline–Amorphous Transitions
inferred← citeshttps://doi.org/10.1002/ceur.202500220openalex-snapshot
Advances in Enaminomaleimides Chemistry: Synthesis, Chemical Applications, and Perspectives
inferred← citeshttps://doi.org/10.1002/chem.201501519openalex-snapshot
Color Tuning of the Aggregation‐Induced Emission of Maleimide Dyes by Molecular Design and Morphology Control
inferred← citeshttps://doi.org/10.1002/chem.201804733openalex-snapshot
Synthesis and Evaluation of a 1,3a,6a‐Triazapentalene (TAP)‐Bonded System
inferred← citeshttps://doi.org/10.1002/ejoc.201701479openalex-snapshot
3,4‐Diaminomaleimide Dyes – Simple Luminophores with Efficient Orange‐Red Emission in the Solid State
inferred← citeshttps://doi.org/10.1002/ejoc.201900195openalex-snapshot
Solid‐State Emissive Diaminomaleimide Dimers and a Polymer – Syntheses, Structures and Optical Properties
inferred← citeshttps://doi.org/10.1002/pi.5740openalex-snapshot
Utilizing functionalized bromomaleimides for fluorogenic conjugation and PEGylation of enzymes
inferred← citeshttps://doi.org/10.1002/slct.202202559openalex-snapshot
Glycolipid‐Type Amphiphiles with a Small Anilinochloromaleimide‐Based Luminogen Exhibiting Aggregation‐Induced Emission
inferred← citeshttps://doi.org/10.1002/slct.202501958openalex-snapshot
Synthesis, Characterization, and Photophysical Investigation of a Dyad Comprising 8‐Methyl‐2‐phenylimidazo[1,2‐ a ]pyridine and N ‐methyl Maleimide for Photoinduced Electron Transfer
inferred← citeshttps://doi.org/10.1016/j.saa.2024.124922openalex-snapshot
Novel thiomaleimide-based fluorescent probe with aggregation-induced emission for detecting H2S
inferred← citeshttps://doi.org/10.1016/j.tet.2014.12.023openalex-snapshot
Facile construction of N-alkyl arylaminomaleimide derivatives as intensively emissive aggregation induced emission dyes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.03.050openalex-snapshot
One-pot synthesis of 3-arylaminomaleimides from terminal alkynes and isocyanates
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00263openalex-snapshot
Aggregation-Induced Emission: Together We Shine, United We Soar!
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02706openalex-snapshot
One-Pot Synthesis and Structure–Property Relationship of Aminomaleimides: Fluorescence Efficiencies in Monomers and Aggregates Easily Tuned by Switch of Aryl and Alkyl
inferred← citeshttps://doi.org/10.1021/acs.jpca.7b04702openalex-snapshot
First Step toward a Universal Fluorescent Probe: Unravelling the Photodynamics of an Amino–Maleimide Fluorophore
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02185openalex-snapshot
Kinetic Resolution Approach to the Synthesis of C–N Axially ChiralN-Aryl Aminomaleimides via NHC-Catalyzed [3 + 3] Annulation
inferred← citeshttps://doi.org/10.1039/c4ra05871bopenalex-snapshot
Aggregation-induced emission active D-π-A binaphthyl luminophore with dual-mode fluorescence
inferred← citeshttps://doi.org/10.1039/c5cc02908bopenalex-snapshot
Aminomaleimide fluorophores: a simple functional group with bright, solvent dependent emission
inferred← citeshttps://doi.org/10.1039/c5ra18690kopenalex-snapshot
Effect of alkyl groups on emission properties of aggregation induced emission active N-alkyl arylaminomaleimide dyes
inferred← citeshttps://doi.org/10.1039/d0qo01285hopenalex-snapshot
Alkylaminomaleimide fluorophores: synthesis via air oxidation and emission modulation by twisted intramolecular charge transfer
inferred← citeshttps://doi.org/10.1039/d1nj04849jopenalex-snapshot
Synthesis and optical properties of conjugated maleimide molecules containing amino with aggregation-induced emission enhancement (AIEE)
inferred← citeshttps://doi.org/10.1039/d3ob00197kopenalex-snapshot
Synthesis of 2-carboxyaniline-substituted maleimides from 2′-nitrochalcones
inferred← citeshttps://doi.org/10.1039/d3ob01765fopenalex-snapshot
Developing a straightforward route toward the synthesis of arylaminomaleimides by palladium-catalyzed arylation of one-pot synthesized aminomaleimides
inferred← citeshttps://doi.org/10.1039/d5ob01392eopenalex-snapshot
Bis-amino maleimides: a new class of dual hydrogen bond donor for anion binding and transport
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.71.880openalex-snapshot
Synthesis of Novel Organoarsenic Compounds and Their Metal Complexes
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