Jingyun Tan

ORCID: 0000-0003-2957-7025
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Luminescence and Fluorescent Materials
  • Molecular Sensors and Ion Detection
  • Synthesis and Properties of Aromatic Compounds
  • Photochromic and Fluorescence Chemistry
  • Crystallography and molecular interactions
  • Nonlinear Optical Materials Studies
  • Supramolecular Self-Assembly in Materials
  • Nonlinear Optical Materials Research
  • Porphyrin and Phthalocyanine Chemistry
  • Click Chemistry and Applications
  • Advanced biosensing and bioanalysis techniques
  • Fullerene Chemistry and Applications
  • Sulfur Compounds in Biology
  • Analytical Chemistry and Sensors
  • Organic Electronics and Photovoltaics
  • Nanowire Synthesis and Applications
  • Nanoplatforms for cancer theranostics
  • Quantum Dots Synthesis And Properties
  • Metal-Organic Frameworks: Synthesis and Applications
  • Photochemistry and Electron Transfer Studies
  • DNA and Nucleic Acid Chemistry
  • Anodic Oxide Films and Nanostructures
  • Nanocluster Synthesis and Applications

Okinawa Institute of Science and Technology Graduate University
2021-2025

University of Macau
2017-2025

Central South University
2021-2023

Faculty of Public Health
2019

Anhui University
2013-2017

Hefei University
2014-2016

Institute of Solid State Physics
2001

Double helicenes are appealing chiral frameworks. Their π-extension is desirable to achieve (chir)optical response in the visible and near-infrared (NIR) region, but access higher double [n]helicenes (n≥8) has remained challenging. Herein, we report an unprecedented π-extended [9]helicene (D9H), unambiguously revealing its structure by single-crystal X-ray diffraction. D9H shows remarkable NIR emission from 750 1100 nm with a high photoluminescence quantum yield of 18 %. In addition,...

10.1002/anie.202218494 article EN Angewandte Chemie International Edition 2023-03-02

Photosensitizers to precise target and change fluorescence upon light illumination could accurately self-report where when the photosensitizers work, enabling us visualize therapeutic process precisely regulate treatment outcomes, which is unremitting pursuit of precision personalized medicine. Here, we report self-immolative by adopting a strategy light-manipulated oxidative cleavage C═C bonds that can generate burst reactive oxygen species, cleave release self-reported red-emitting...

10.1021/jacs.3c01666 article EN Journal of the American Chemical Society 2023-05-22

Abstract A negatively curved aza‐nanographene (NG) containing two octagons was synthesized by a regioselective and stepwise cyclodehydrogenation procedure, in which double aza[7]helicene simultaneously formed as an intermediate. Their saddle‐shaped structures with negative curvature were unambiguously confirmed X‐ray crystallography, thereby enabling the exploration of structure–property relationship photophysical, electrochemical conformational studies. Moreover, assembly octagon‐embedded...

10.1002/anie.202400172 article EN Angewandte Chemie International Edition 2024-02-12

This work describes a facile yet powerful approach to energy-transfer NMOF (nanoscale metal–organic framework) fabrication for ratiometric peroxynitrite (ONOO<sup>−</sup>) sensing.

10.1039/c7sc01077j article EN cc-by-nc Chemical Science 2017-01-01

A chiral amino acid functionalized probe, PTZ-D, could self-assemble into a organogel displaying unprecedented chiroptical monitoring of ClO<sup>−</sup> with switchable CPL signals.

10.1039/c9cc05245c article EN Chemical Communications 2019-01-01

Abstract Imaging abnormal copper/iron with effective fluorescent tools is essential to comprehensively put insight into many pathological events. However, conventional coordination‐based detection mired in the fluorescence quenching induced by paramagnetic Cu(II)/Fe(III). Moreover, strong chelating property of probe will consume dissociative metal ions and inevitably interfere physiological microenvironment. Here, a new strategy developed employing this aberrant Cu(II)/Fe(III) catalyze bond...

10.1002/advs.202412407 article EN cc-by Advanced Science 2025-01-09

A benzo[ rst ]pentaphene (BPP) substituted by an isopropoxy group (BPP-OiPr) was synthesized in a facile manner. Its photophysical properties were investigated UV–vis absorption and fluorescence spectroscopy compassion to pristine BPP its oxidation product, ]pentaphene-5,8-dione (BPP-dione). BPP-OiPr exhibited significantly enhanced photoluminescence quantum yield (PLQY), reaching 73% comparison (13%). BPP-dione, when compared the parent BPP, also displayed improved emission from first...

10.3762/bjoc.21.19 article EN cc-by Beilstein Journal of Organic Chemistry 2025-02-04

Six thiophene-based chalcone derivatives were synthesized, and their structure–property relationship was investigated systematically. Small molecules as they are, have showed favorable <italic>Φ</italic> <italic>σ</italic> values in the near-IR region.

10.1039/c6tc00382f article EN Journal of Materials Chemistry C 2016-01-01

Reductive cleavage of alkenes is rarely reported in synthetic chemistry. Here we report a unique H2S-mediated reductive C[double bond, length as m-dash]C bonds under mild conditions, which successful new strategy for the design probes effective sensing H2S with turn-on dual-color fluorescence. A short series phenothiazine ethylidene malononitrile derivatives were shown to react H2S, via intramolecular cyclization reactions form thiophene rings. Enlightened by this reaction mechanism, four...

10.1039/c8sc03430c article EN cc-by-nc Chemical Science 2018-01-01

The crystal structures of a thiophene-based terpyridine ligand and its four zinc halide complexes had been discussed. open-aperture <italic>Z</italic>-scan results showed that <bold>LZnBr2</bold> exhibits the best two-photon absorption property, which is greatly superior to free <bold>L</bold>.

10.1039/c4dt02933j article EN Dalton Transactions 2014-11-19

Herein we present a synthesis of an S-shaped double helicene with fused imide moieties, achieving contorted aromatic diimide (DHDI) good fluorescence properties in both solution and the solid state. DHDI demonstrates distinct mechanofluorochromism from yellow to green emission under grinding its crystalline powder.

10.1021/acs.orglett.1c00678 article EN Organic Letters 2021-04-19

Abstract The development of helicenes with strong chiroptical response and controlled photophysics is highly desirable but challenging. In this work, double thia/sulfone[7]helicenes were synthesized to investigate the heteroatom effect on photophysical properties heterohelicenes through comparison previously reported oxa[7]helicene. By variation embedded heteroatoms from oxygen sulfur, absorption emission significantly red‐shifted, along improved luminescence dissymmetry factor ( g lum )....

10.1002/asia.202200336 article EN Chemistry - An Asian Journal 2022-05-31

Abstract Double helicenes are appealing chiral frameworks. Their π‐extension is desirable to achieve (chir)optical response in the visible and near‐infrared (NIR) region, but access higher double [ n ]helicenes ( ≥8) has remained challenging. Herein, we report an unprecedented π‐extended [9]helicene D9H ), unambiguously revealing its structure by single‐crystal X‐ray diffraction. shows remarkable NIR emission from 750 1100 nm with a high photoluminescence quantum yield of 18 %. In addition,...

10.1002/ange.202218494 article EN Angewandte Chemie 2023-03-02

The synthesis of a class contorted electron-deficient polycyclic aromatic hydrocarbons (PAHs) has been achieved by one-pot bay annulation perylene diimide involving mild Suzuki coupling and subsequent air-mediated, ambient-light-induced photocyclization. X-ray crystallography unambiguously confirmed the PAH structure bearing four imide groups. photophysical electronic properties these PAHs were also analyzed, showing high fluorescence quantum yield 86% moderate electron mobility 0.017 cm2 V-1 s-1.

10.1021/acs.orglett.2c00690 article EN Organic Letters 2022-03-18

This contribution describes an efficient approach to constructing chiral spiro[pyrrol-benzopyran] (SPP) scaffold with high asymmetry. By combining SPP and the achiral sensing moiety phenothiazine, target probe P showed unprecedented reaction-based chiroptical towards hypochlorite switching CD signals.

10.1039/c9cc02946j article EN Chemical Communications 2019-01-01

Abstract Cadmium sulfide (CdS) nanowire was synthesized by a convenient ultraviolet irradiation method using hydroxyethyl cellulose as soft template at room temperature.

10.1246/cl.2001.396 article EN Chemistry Letters 2001-05-01
Coming Soon ...