[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Bai et al., 2022 - Google Patents

Precise probe design based ESIPT coupled AIE mechanism toward endogenous cyanide in food detection and bioimaging

Bai et al., 2022

View PDF
Document ID
1444690750249408571
Author
Bai C
Zhang J
Qin Y
Huang H
Xia Z
Zheng Q
Dai H
Lu P
Miao H
Qu C
Qiao R
Publication year
Publication venue
Chemical Engineering Journal

External Links

Snippet

Cyanide (CN–) is one of the strongest and fastest-acting toxic substances, and its excessive presence will cause great harm to the environment, food and human health. Although several fluorescent probes that recognize CN–have been extensively reported, developing …
Continue reading at papers.ssrn.com (PDF) (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
    • C07D487/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains four or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using infra-red, visible or ultra-violet light
    • G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1003—Carbocyclic compounds
    • C09K2211/1007—Non-condensed systems

Similar Documents

Publication Publication Date Title
Bai et al. Precise probe design based ESIPT coupled AIE mechanism toward endogenous cyanide in food detection and bioimaging
Fu et al. A colorimetric and fluorescent sensor for Cu2+ and F− based on a diarylethene with a 1, 8-naphthalimide Schiff base unit
Liao et al. A novel acylhydrazone-based derivative as dual-mode chemosensor for Al3+, Zn2+ and Fe3+ and its applications in cell imaging
Erdemir Fluorometric dual sensing of Hg2+ and Al3+ by novel triphenylamine appended rhodamine derivative in aqueous media
Qiu et al. An unusual AIE fluorescent sensor for sequentially detecting Co2+-Hg2+-Cu2+ based on diphenylacrylonitrile Schiff-base derivative
Grabchev et al. Synthesis and photophysical properties of 1, 8-naphthalimide-labelled PAMAM as PET sensors of protons and of transition metal ions
Chen et al. A highly selective naked-eye and fluorescent probe for fluoride ion based on 1, 8-naphalimide and benzothizazole
Zhang et al. A Highly Fluorescent Anthracene‐Containing Hybrid Material Exhibiting Tunable Blue–Green Emission Based on the Formation of an Unusual “T‐Shaped” Excimer
Alamry et al. A ratiometric rhodamine–naphthalimide pH selective probe built on the basis of a PAMAM light-harvesting architecture
Wang et al. Rhodamine-2-thioxoquinazolin-4-one conjugate: A highly sensitive and selective chemosensor for Fe3+ ions and crystal structures of its Ag (I) and Hg (II) complexes
Qin et al. A novel ratiometric fluorescent probe for detection of Fe3+ by rhodamine–quinoline conjugate
Liu et al. Circularly polarized luminescence from axially chiral binaphthalene-bridged BODIPY
Mehdi et al. Aggregation‐Induced Emission (AIE) Fluorophore Exhibits a Highly Ratiometric Fluorescent Response to Zn2+ in vitro and in Human Liver Cancer Cells
Wang et al. Novel ‘naked-eye’Bis-Schiff base fluorescent chemosensors for sensitive detection of Zn2+ and bio-imaging in living cells
Chen et al. A versatile aggregation‐induced emission fluorescent probe for visible detection of pH
Guo et al. A colorimetric and fluorescent chemosensor for Hg 2+ based on a photochromic diarylethene with a quinoline unit
Wang et al. ACQ-to-AIE conversion by regio-isomerization of rofecoxib analogues for developing new multi-functional aggregation-induced emission luminogens
Tang et al. An o-hydroxyl aldehyde structure based naphthalimide derivative: Reversible photochromic properties and its application in ClO− detection in living cells
Dong et al. Highly selective and sensitive fluorometric probe for Cd2+ ions based on 4-(quinolin-2-ylmethylene) aminoanisole Schiff base
Wang et al. Selective sensing of PPi by fluorogenic Al (III)-probe complex in aqueous medium
Bai et al. Novel fluorescent probe for sequential recognition of Zn2+ and pyrophosphate in aqueous based on aggregation-induced emission
Çamur et al. Synthesis, characterization and fluorescence behavior of new fluorescent probe phthalocyanines bearing coumarin substituents
Hu et al. “AIE+ ESIPT” bis Schiff-base ligands with multicolor emission and their corresponding Eu (III) complexes: Synthesis and properties research
Wu et al. Multi-stimuli-responsive fluorescence of axially chiral 4-ene-β-Diketones
Shanmugapriya et al. An indolinium-based chemo-dosimeter for highly selective dual-channel detection of cyanide ion: A combined experimental and theoretical investigations