On the public citation graph
The Solvatofluorochromism of 2,4,6‐Triarylpyrimidine Derivatives
0 signed · 60 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/adom.201600843openalex-snapshot
Significant Enhancement of Blue OLED Performances through Molecular Engineering of Pyrimidine‐Based Emitter
inferredcites →https://doi.org/10.1002/aoc.2865openalex-snapshot
Double Suzuki cross‐coupling reaction of pyrimidine boronic acid: synthesis of new versatile dielectrophile
inferredcites →https://doi.org/10.1002/ejoc.201001622openalex-snapshot
Synthesis and Photophysical Properties of Alkynylated Pyrimidines by Site‐Selective Sonogashira Reactions of 2,4,5,6‐Tetrachloropyrimidine; First Synthesis of Tetraalkynyl‐pyrimidines
inferredcites →https://doi.org/10.1002/hlca.201400168openalex-snapshot
Synthesis of 3,5‐Diarylcyclohex‐2‐enones by NH4Cl/HCl‐Catalyzed Cyclization and Deacetylation of 4‐Acetylhexane‐1,5‐diones
inferredcites →https://doi.org/10.1002/slct.201702472openalex-snapshot
Photoluminescence Properties of Aryl‐, Arylvinyl‐, and Arylethynylpyrimidine Derivatives
inferredcites →https://doi.org/10.1007/s00216-016-9501-4openalex-snapshot
Detection of nitroaromatic explosives by new D–π–A sensing fluorophores on the basis of the pyrimidine scaffold
inferredcites →https://doi.org/10.1016/0301-0104(94)00256-8openalex-snapshot
Excited charge transfer states in 4-aminopyrimidines, 4-(dimethylanilino)pyrimidine and 4-(dimethylamino)pyridne
inferredcites →https://doi.org/10.1016/j.arabjc.2010.10.034openalex-snapshot
Synthesis, spectral studies, antimicrobial and insect antifeedant activities of some substituted styryl 4′-fluorophenyl ketones
inferredcites →https://doi.org/10.1016/j.bmc.2014.05.037openalex-snapshot
SAR studies of differently functionalized chalcones based hydrazones and their cyclized derivatives as inhibitors of mammalian cathepsin B and cathepsin H
inferredcites →https://doi.org/10.1016/j.foodchem.2015.07.036openalex-snapshot
Location of TEMPO derivatives in micelles: subtle effect of the probe orientation
inferredcites →https://doi.org/10.1016/j.foodchem.2017.10.094openalex-snapshot
Antioxidant-spotting in micelles and emulsions
inferredcites →https://doi.org/10.1016/j.jphotochem.2017.08.060openalex-snapshot
Emission properties of diazines chromophores: Structure-properties relationship
inferredcites →https://doi.org/10.1016/j.molliq.2013.03.018openalex-snapshot
Solvatochromic fluorescence behavior of 2-amino-6-hydroxy-4-(3,4-dimethoxyphenyl)-pyrimidine-5-carbonitrile: A sensitive fluorescent probe for detection of pH and water composition in binary aqueous solutions
inferredcites →https://doi.org/10.1016/j.tet.2008.01.037openalex-snapshot
Bis- and tris(arylethynyl)pyrimidine oligomers: synthesis and light-emitting properties
inferredcites →https://doi.org/10.1016/j.tet.2010.10.059openalex-snapshot
Synthesis of nitrogen bicyclic scaffolds: pyrimido[1,2-a]pyrimidine-2,6-diones
inferredcites →https://doi.org/10.1016/j.tetlet.2013.06.040openalex-snapshot
2-Arylvinylpyrimidines versus 4-arylvinylpyrimidines: synthesis and comparison of the optical properties
inferredcites →https://doi.org/10.1021/acs.joc.7b01442openalex-snapshot
Dipolar NLO Chromophores Bearing Diazine Rings as π-Conjugated Linkers
inferredcites →https://doi.org/10.1021/cc049910topenalex-snapshot
Traceless Solid-Phase Synthesis of Nitrogen-Containing Heterocycles and Their Biological Evaluations as Inhibitors of Neuronal Sodium Channels
inferredcites →https://doi.org/10.1021/ct300326fopenalex-snapshot
TD-DFT Assessment of Functionals for Optical 0–0 Transitions in Solvated Dyes
inferredcites →https://doi.org/10.1021/j100162a011openalex-snapshot
"Twisted" intramolecular charge-transfer states in supercooled molecules: structural effects and clustering with polar molecules
inferredcites →https://doi.org/10.1021/j100346a015openalex-snapshot
Dual fluorescence of 4-(dialkylamino)pyrimidines. Twisted intramolecular charge transfer state formation favored by hydrogen bond or by coordination to the metal ion
inferredcites →https://doi.org/10.1021/ja044923wopenalex-snapshot
Pyrimidine-Core Extended π-Systems: General Synthesis and Interesting Fluorescent Properties
inferredcites →https://doi.org/10.1021/jo200204uopenalex-snapshot
4-Arylvinyl-2,6-di(pyridin-2-yl)pyrimidines: Synthesis and Optical Properties
inferredcites →https://doi.org/10.1021/jo3004919openalex-snapshot
Synthesis and Photophysical Investigation of a Series of Push–Pull Arylvinyldiazine Chromophores
inferredcites →https://doi.org/10.1021/jo301675gopenalex-snapshot
Stereoselective and Catalytic Access to β-Enaminones: An Entry to Pyrimidines
inferredcites →https://doi.org/10.1021/jo900107uopenalex-snapshot
V-Shaped 4,6-Bis(arylvinyl)pyrimidine Oligomers: Synthesis and Optical Properties
inferredcites →https://doi.org/10.1021/jp8095727openalex-snapshot
Toward a Generalized Treatment of the Solvent Effect Based on Four Empirical Scales: Dipolarity (SdP, a New Scale), Polarizability (SP), Acidity (SA), and Basicity (SB) of the Medium
inferredcites →https://doi.org/10.1039/b702004jopenalex-snapshot
Novel pyrimidine-based amphiphilic molecules: synthesis, spectroscopic properties and applications in two-photon fluorescence microscopic imaging
inferredcites →https://doi.org/10.1039/c3ra43631dopenalex-snapshot
Bipolar luminescent materials containing pyrimidine terminals: synthesis, photophysical properties and a theoretical study
inferredcites →https://doi.org/10.1039/c3ra44357dopenalex-snapshot
Hierarchically structured graphene-based supercapacitor electrodes
inferredcites →https://doi.org/10.1039/c5ra16995jopenalex-snapshot
Direct access to pyrimidines through organocatalytic inverse-electron-demand Diels–Alder reaction of ketones with 1,3,5-triazine
inferredcites →https://doi.org/10.1055/s-0036-1588810openalex-snapshot
Microwave-Promoted Synthesis of 4-Arylpyrimidines by Pd-Catalysed Suzuki–Miyaura Coupling of 4-Pyrimidyl Tosylates in Water
inferredcites →https://doi.org/10.3762/bjoc.10.37openalex-snapshot
The Flögel-three-component reaction with dicarboxylic acids – an approach to bis(β-alkoxy-β-ketoenamides) for the synthesis of complex pyridine and pyrimidine derivatives
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4783683openalex-extracted
Photophysical properties of 6-arylvinyl-2,4-bis(2′-hydroxyphenyl)pyrimidines ligands and their boron fluoride complexes
inferred← citeshttps://doi.org/10.1002/chem.202000817openalex-snapshot
Push–Pull (Iso)quinoline Chromophores: Synthesis, Photophysical Properties, and Use for White‐Light Emission
inferred← citeshttps://doi.org/10.1002/chem.202501089openalex-snapshot
Pyrimidine‐Based Four‐Coordinate O^N^O Boron Complexes: Synthesis, Photophysical and Theoretical Studies, and TADF‐Based OLED Devices
inferred← citeshttps://doi.org/10.1002/cptc.202300085openalex-snapshot
Aggregation‐Induced Enhanced Emission of a Dimethylacridan Substituted Pyrimidine Derivative
inferred← citeshttps://doi.org/10.1002/ejoc.202000870openalex-snapshot
Electron‐Withdrawing Substituted Quinazoline Push‐Pull Chromophores: Synthesis, Electrochemical, Photophysical and Second‐Order Nonlinear Optical Properties
inferred← citeshttps://doi.org/10.1002/jhet.4768openalex-snapshot
4‐substituted push‐pull quinazoline chromophores with extended π‐conjugated linker
inferred← citeshttps://doi.org/10.1002/slct.202103280openalex-snapshot
Reactivity of 4‐pyrimidyl Sulfonic Esters in Suzuki‐Miyaura Cross‐Coupling Reactions in Water Under Microwave Irradiation
inferred← citeshttps://doi.org/10.1007/s13738-023-02888-6openalex-snapshot
Synthesis of novel triarylmethane derivatives containing a trichloropyrimidine moiety
inferred← citeshttps://doi.org/10.1016/j.dyepig.2019.03.054openalex-snapshot
Solvatofluorochromism of conjugated 4-methoxyphenyl-Pyridinium electron donor-acceptor pairs
inferred← citeshttps://doi.org/10.1016/j.dyepig.2020.108659openalex-snapshot
Nonlinear optical properties of pyrimidine chromophores
inferred← citeshttps://doi.org/10.1016/j.dyepig.2020.108948openalex-snapshot
Effect of protonation on the photophysical properties of 4-substituted and 4,7-disubstituted quinazoline push-pull chromophores
inferred← citeshttps://doi.org/10.1016/j.dyepig.2022.110949openalex-snapshot
The role of acceptor and π-bridge for donor-driven halochromism of D-π-A N,N-dialkylaminostyrylhetarenes
inferred← citeshttps://doi.org/10.1016/j.dyepig.2025.112660openalex-snapshot
Synthesis and photophysical properties of 6-aryl-2,4-bis(2′-hydroxyphenyl)pyrimidines ligands and their boron fluoride complexes
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2020.112900openalex-snapshot
Synthesis, photophysical and nonlinear optical properties of [1,2,5]oxadiazolo[3,4-b]pyrazine-based linear push-pull systems
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2021.113311openalex-snapshot
Synthesis, photophysical, thermal properties and X-Ray studies of novel organic dyes bearing Inden-1-ylidene and fluorene
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.120784openalex-snapshot
Extending the π-system of inverted solvatochromic phenolate-based dyes shifts their inversion point due to an increment in their sensitivity to solvent polarizability
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.133909openalex-snapshot
Site-selective nucleophilic substitution reactions of 2,4,5,6-tetrachloropyrimidine with sulfonamides: Synthesis of novel trichloropyrimidine-arylsulfonamide hybrid derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.137627openalex-snapshot
Intramolecular charge transfer character of D-π-A chromophores with modulating the subunits sequence of π-bridge
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.147599openalex-snapshot
Positive fluorosolvatochromism in N,N-dimethyl-4-amino-2,1,3-benzothiadiazole: A polarity-sensitive fluorescent probe
inferred← citeshttps://doi.org/10.1021/acs.jpca.5c06504openalex-snapshot
Excited-State Relaxation Pathways of 4-Aminobiphenyl-2-Pyrimidine Derivatives: An Ultrafast Perspective
inferred← citeshttps://doi.org/10.1021/acsaom.4c00251openalex-snapshot
Tunable Emission and Structural Insights of 6-Arylvinyl-2,4-bis(2′-hydroxyphenyl)pyrimidines and Their O∧N∧O-Chelated Boron Complexes
inferred← citeshttps://doi.org/10.1039/c9cp06476aopenalex-snapshot
Branching effect on the linear and nonlinear optical properties of styrylpyrimidines
inferred← citeshttps://doi.org/10.1039/d1se00387aopenalex-snapshot
A benzofuran[ b ]-fused BODIPY as an efficient sensitizer for photocatalytic hydrogen production
inferred← citeshttps://doi.org/10.1246/bcsj.20190101openalex-snapshot
A Series of 2,5-Bis(5-aryl-2-thienyl)pyrazines with a Linear-Shaped (D-π)2-A System: Synthesis and Study of the Optical Properties Including Fluorosolvatochromism and Proton-Base-Sensing
inferred← citeshttps://doi.org/10.3389/fchem.2023.1292541openalex-snapshot
Governing the emissive properties of 4-aminobiphenyl-2-pyrimidine push–pull systems via the restricted torsion of N,N-disubstituted amino groups
inferred← citeshttps://doi.org/10.3390/molecules24091742openalex-snapshot
Carbazole- and Triphenylamine-Substituted Pyrimidines: Synthesis and Photophysical Properties
inferred← citeshttps://doi.org/10.3390/molecules27249023openalex-snapshot
Computational Quantification of the Zwitterionic/Quinoid Ratio of Phenolate Dyes for Their Solvatochromic Prediction
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.