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Signal Processing at the Molecular Level
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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The unimolecular rectifier: unimolecular electronic devices are coming …
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All about (N-hexadecylquinolin-4-ium-1-yl)methylidenetricyanoquinodimethanide, a unimolecular rectifier of electrical current
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A [2]Catenane-Based Solid State Electronically Reconfigurable Switch
What points at this work
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The synthesis and spectroscopic properties of novel, photochromic indolinobenzospiropyran-based homopolymers prepared via ring-opening metathesis polymerization
inferred← citeshttps://doi.org/10.1016/j.dyepig.2010.03.018openalex-snapshot
Toward multi-addressable molecular systems: Efficient synthesis and photochromic performance of unsymmetrical bisthienylethenes
inferred← citeshttps://doi.org/10.1016/j.dyepig.2011.03.021openalex-snapshot
Spiropyran, chromene and spirooxazine, mélange á trois: Molecular logic systems through selective and reversible deactivation of photochromism mediated by CO2 gas
inferred← citeshttps://doi.org/10.1016/j.dyepig.2012.04.020openalex-snapshot
Synthesis of ru(bpy)3-viologen and its complex included by p-sulfonatocalix[4]arene in a U-type binding manner
inferred← citeshttps://doi.org/10.1016/j.dyepig.2014.12.008openalex-snapshot
Synthesis of amphiphilic spiropyran-based random copolymer by atom transfer radical polymerization for Co2+ recognition
inferred← citeshttps://doi.org/10.1016/j.dyepig.2016.08.039openalex-snapshot
Diversely halogenated spiropyrans - Useful synthetic building blocks for a versatile class of molecular switches
inferred← citeshttps://doi.org/10.1016/j.dyepig.2019.107778openalex-snapshot
A novel and durable photochromic cotton-based fabric prepared via thiol-ene click chemistry
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2017.01.033openalex-snapshot
Engineering of new spiropyran photochromic fluorescent polymeric nanoparticles of narrow size distribution by emulsion polymerization process
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2026.114628openalex-snapshot
Stimuli-responsive chromism in sensor applications: A review
inferred← citeshttps://doi.org/10.1016/j.ica.2006.07.029openalex-snapshot
Nanoparticle-induced transition from positive to negative photochromism
inferred← citeshttps://doi.org/10.1016/j.ica.2011.09.003openalex-snapshot
Cryptand receptors in metal ion induced fluorescence signaling
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.117524openalex-snapshot
Positive and negative photochromic and fluorescent color-changing cotton fabrics for information switching and encryption
inferred← citeshttps://doi.org/10.1016/j.jcis.2023.11.024openalex-snapshot
Preparation and dynamic color-changing study of fluorescent polymer nanoparticles for individualized and customized anti-counterfeiting application
inferred← citeshttps://doi.org/10.1016/j.jconrel.2017.08.013openalex-snapshot
The integration of triggered drug delivery with real time quantification using FRET; creating a super ‘smart’ drug delivery system
inferred← citeshttps://doi.org/10.1016/j.jlumin.2004.04.009openalex-snapshot
Cryptand-based fluorescent signaling systems: high enhancement with transition, inner-transition as well as heavy main-group metal ions
inferred← citeshttps://doi.org/10.1016/j.jlumin.2016.07.028openalex-snapshot
Photoswitchable conjugated assembly involving fluorescent boranil
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2010.05.012openalex-snapshot
Reverse photochromism of spiropyran in silica
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2010.05.024openalex-snapshot
Reversible multi-coloring reaction of spironaphtooxazine controlled by long-chain molecule
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2012.04.003openalex-snapshot
Colorimetric detection of aliphatic primary amines and a molecular logic gate based on a photochromic phenoxyquinone derivative
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2013.04.017openalex-snapshot
Photo-induced reversible proton dissociation of spirobenzopyran in aqueous systems
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2024.116081openalex-snapshot
A novel merocyanine photoacid for visible light-controlled pH modulation
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2025.116727openalex-snapshot
Interplay of solvent polarity and hydrogen bonding in thermal isomerization of spiropyran
inferred← citeshttps://doi.org/10.1016/j.mencom.2023.06.021openalex-snapshot
Electrochemical investigation of a photochromic spiropyran containing a pyrrolidinofullerene moiety
inferred← citeshttps://doi.org/10.1016/j.micromeso.2008.08.040openalex-snapshot
Synthesis of silica spheres with neutral and ionic amphiphiles and their interaction with photosensitive spiropyrans
inferred← citeshttps://doi.org/10.1016/j.micromeso.2024.113084openalex-snapshot
Stable Ring-Opened Forms of a Spiropyran in the Confined Space of Nanoporous Silicas
inferred← citeshttps://doi.org/10.1016/j.mtchem.2026.103580openalex-snapshot
“All roads lead to Rome's” thermoresponsive luminescence of D-π-A carbazolyl-difluoroboron-β-diketonate toward programmable photonic circuits-based temperature sensor
inferred← citeshttps://doi.org/10.1016/j.poly.2009.06.050openalex-snapshot
Polarized spectroscopy of hybrid materials of chiral Schiff base cobalt(II), nickel(II), copper(II), and zinc(II) complexes and photochromic azobenzenes in PMMA films
inferred← citeshttps://doi.org/10.1016/j.polymer.2006.08.066openalex-snapshot
Photoresponsive polymers: An investigation of their photoinduced temperature changes during photoviscosity measurements
inferred← citeshttps://doi.org/10.1016/j.polymer.2015.01.068openalex-snapshot
Synthesis and characterization of new spiropyran micrometer-sized photochromic fluorescent polymeric particles of narrow size distribution by a swelling process
inferred← citeshttps://doi.org/10.1016/j.polymer.2015.12.027openalex-snapshot
A photo, temperature, and pH responsive spiropyran-functionalized polymer: Synthesis, self-assembly and controlled release
inferred← citeshttps://doi.org/10.1016/j.polymer.2016.08.082openalex-snapshot
RAFT alcoholic dispersion polymerization with polymerization-induced self-assembly
inferred← citeshttps://doi.org/10.1016/j.porgcoat.2021.106259openalex-snapshot
pH-responsive spiropyran-based copolymers and their application in monitoring and antibacterial coatings
inferred← citeshttps://doi.org/10.1016/j.porgcoat.2021.106531openalex-snapshot
Sunlight-induced photo-thermochromic smart window based spiropyran-functionalized copolymer for UV shielding and sunlight management
inferred← citeshttps://doi.org/10.1016/j.porgcoat.2022.106847openalex-snapshot
Photo- and thermo-responsive extracellular matrix mimicking nano-coatings prepared from poly(N-isopropylacrylamide)-spiropyran copolymer for effective cell sheet harvesting
inferred← citeshttps://doi.org/10.1016/j.proche.2014.12.039openalex-snapshot
Electrochemical Characterization of Spiropyran Structures
inferred← citeshttps://doi.org/10.1016/j.progpolymsci.2017.06.002openalex-snapshot
Light-induced release of molecules from polymers
inferred← citeshttps://doi.org/10.1016/j.progpolymsci.2019.101149openalex-snapshot
Stimuli-chromism of photoswitches in smart polymers: Recent advances and applications as chemosensors
inferred← citeshttps://doi.org/10.1016/j.reactfunctpolym.2012.04.011openalex-snapshot
Synthesis and photoresponsive behavior of optically active methacrylic homopolymers containing side-chain spiropyran chromophores
inferred← citeshttps://doi.org/10.1016/j.rechem.2021.100106openalex-snapshot
Photoactivatable 1,2-dioxetane chemiluminophores
inferred← citeshttps://doi.org/10.1016/j.saa.2013.08.005openalex-snapshot
Synthesis and solvent-dependent photochromic reactions of porphyrin–spiropyran hybrid compounds
inferred← citeshttps://doi.org/10.1016/j.saa.2015.03.082openalex-snapshot
Three novel input logic gates supported by fluorescence studies: Organic nanoparticles (ONPs) as chemo-sensor for detection of Zn2+ and Al3+ in aqueous medium
inferred← citeshttps://doi.org/10.1016/j.saa.2015.06.021openalex-snapshot
A dithienosilole-based fluorescent chemosensor for multiple logic operations at the molecular level
inferred← citeshttps://doi.org/10.1016/j.saa.2018.04.076openalex-snapshot
Substituent effect on the acid-induced isomerization of spiropyran compounds
inferred← citeshttps://doi.org/10.1016/j.saa.2020.119385openalex-snapshot
Spiropyran based recognitions of amines: UV–Vis spectra and mechanisms
inferred← citeshttps://doi.org/10.1016/j.snb.2008.03.029openalex-snapshot
Three-input chemical logic circuits based on a new fluorescent sensor for ATP and Cu2+in aqueous solution
inferred← citeshttps://doi.org/10.1016/j.snb.2016.03.039openalex-snapshot
A new molecular logic circuit with 4 bit input
inferred← citeshttps://doi.org/10.1016/j.snb.2017.03.140openalex-snapshot
Ciprofloxacin as chemosensor for simultaneous recognition of Al3+ and Cu2+ by Logic Gates supported fluorescence: Application to bio-imaging for living cells
inferred← citeshttps://doi.org/10.1016/j.surfin.2025.107712openalex-snapshot
One-step fabrication of durable, self-cleaning, anti-icing and UV-shielding coatings
inferred← citeshttps://doi.org/10.1016/j.tet.2004.04.073openalex-snapshot
Fluorescence emission control and switching of oxymethylcrowned spirobenzopyrans by metal ion
inferred← citeshttps://doi.org/10.1016/j.tet.2004.09.065openalex-snapshot
Photoinduced proton exchange between molecular switches
inferred← citeshttps://doi.org/10.1016/j.tet.2005.05.043openalex-snapshot
Luminescent sensors and switches in the early 21st century
inferred← citeshttps://doi.org/10.1016/j.tet.2006.01.073openalex-snapshot
A selective colorimetric chemosensor for lanthanide ions
inferred← citeshttps://doi.org/10.1016/j.tet.2006.08.061openalex-snapshot
Multi-state molecular switches based on dithienylperfluorocyclopentene and imidazo [4,5-f] [1,10] phenanthroline
inferred← citeshttps://doi.org/10.1016/j.tet.2008.12.020openalex-snapshot
Synthesis and characterization of a redox- and light-sensitive MRI contrast agent
inferred← citeshttps://doi.org/10.1016/j.tet.2010.07.035openalex-snapshot
A photoswitchable Zn (II) selective spiropyran-based sensor
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.11.164openalex-snapshot
Photo-switchable molecular devices based on metal-ionic recognition
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.10.069openalex-snapshot
Functionalization of aminocrown ethers with [2H]-chromene units by Buchwald–Hartwig C–N coupling for constructing of photoswitchable molecular devices
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.12.133openalex-snapshot
A new fluorescent chemosensor for copper(II) and molecular switch controlled by light
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.04.127openalex-snapshot
A FRET fluorescent chemosensor SPAQ for Zn2+ based on a dyad bearing spiropyran and 8-aminoquinoline unit
inferred← citeshttps://doi.org/10.1016/s0009-2614(03)00927-8openalex-snapshot
Reversible modulation of the fluorescence of pyrenemethylamine hydrochloride by light in the presence of spiropyran: signal communication between two molecular switches through proton transfer
inferred← citeshttps://doi.org/10.1021/ac503240xopenalex-snapshot
Selective Tracking of Lysosomal Cu2+ Ions Using Simultaneous Target- and Location-Activated Fluorescent Nanoprobes
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