Yanhua Yang

ORCID: 0000-0003-0482-4552
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Luminescence and Fluorescent Materials
  • Molecular Sensors and Ion Detection
  • Forensic Fingerprint Detection Methods
  • Organic Light-Emitting Diodes Research
  • Advanced Memory and Neural Computing
  • Organic Electronics and Photovoltaics
  • Nanoplatforms for cancer theranostics
  • Conducting polymers and applications
  • Porphyrin and Phthalocyanine Chemistry
  • Advanced machining processes and optimization
  • Semiconductor materials and devices
  • Synthesis and properties of polymers
  • Photochromic and Fluorescence Chemistry
  • Analytical Chemistry and Sensors
  • Fluorine in Organic Chemistry
  • Advanced Surface Polishing Techniques
  • Perovskite Materials and Applications
  • Advanced ceramic materials synthesis
  • Innovative concrete reinforcement materials
  • Advanced biosensing and bioanalysis techniques
  • Polydiacetylene-based materials and applications
  • Synthesis of Indole Derivatives
  • Advanced Machining and Optimization Techniques
  • Organoboron and organosilicon chemistry
  • Magnesium Alloys: Properties and Applications

Kunming University
2020-2025

Dongguan People’s Hospital
2025

Southern Medical University
2025

Yunnan Metallurgical Group (China)
2025

Shandong Transportation Research Institute
2024

Nanjing University of Aeronautics and Astronautics
2018-2020

Chinese University of Hong Kong
2017-2019

Tianjin Research Institute of Water Transport Engineering
2018

Sun Yat-sen University
2017

South China University of Technology
2011

Three dithio-fused boron dipyrromethenes (BODIPYs), DTFB-1, DTFB-2, and DTFB-3, in which symmetrically S-heteroaromatic ring units fused at [a], zigzag, [b] bonds of the parent BODIPY core, respectively, were prepared from facile efficient post-functionalization tetra-halogenated BODIPYs through Pd-catalyzed cyclization. Dithio-fusion various positions effectively tunes their photophysical properties single-crystal structural packing arrangements. The single-crystalline microribbons DTFB-2...

10.1021/acs.orglett.4c01757 article EN Organic Letters 2024-06-24

To further explore the relationship between aryl substituents and mechanofluorochromic (MFC) behaviors, four salicylaldimine-based difluoroboron complexes (ts-Ph BF

10.1002/bio.4729 article EN Luminescence 2024-03-28

A simple synthetic approach to aromatic heterocyclic [ a ]-fused BODIPYs, which exhibit “butterfly-shaped” crystal structures, high Φ F , and tunable HOMO levels.

10.1039/d4qm00616j article EN Materials Chemistry Frontiers 2024-01-01

A pyridine-based difluoroboron compound with the TPA group displayed excellent AIEE activity and MFC behavior, which was applied for latent fingerprint detection inkless writing.

10.1039/d3nj04954j article EN New Journal of Chemistry 2023-12-08

Contrast-induced nephropathy (CIN) is an acute kidney injury manifests within 72 h post-administration of contrast media, excluding other kidney-damage etiologies. Despite the recognition CIN, complex interplay among high-risk factors remains poorly understood, and precision in existing risk stratification models lacking. This retrospective, observational cohort study included patients who underwent percutaneous coronary intervention (PCI) or computed tomography angiography (CTA) at four...

10.1038/s41598-025-91986-x article EN cc-by-nc-nd Scientific Reports 2025-02-26

To further promote the development of multifunctional organoboron fluorescent dyes, three different methyl-substituted pyridine-based difluoroboron compounds (1-BF2, 2-BF2, and 3-BF2) were designed successfully synthesized to explore their photoluminescence properties...

10.1039/d5nj00511f article EN New Journal of Chemistry 2025-01-01

We present a new, straightforward, and versatile approach that utilizes regioselective brominated precursors to synthesize both asymmetric symmetric S-zig-zag-fused BODIPYs (s-TFB bis-TFB) in moderate yields (45% 40%, respectively). X-ray structure analyses reveal the planar rigidity of BODIPY skeleton is progressively enhanced with an increasing number thiopyran rings. The annulation S-heteroaromatic rings at zig-zag edge core results blue-shifted absorption emission spectra, bis-TFB...

10.1021/acs.joc.5c00508 article EN The Journal of Organic Chemistry 2025-04-18

Abstract To further explore the relationship between structure and property of mechanofluorochromic materials, two indole‐based aggregation‐induced emission compounds ( I−Ph−BF 2 I−PhNp−BF ) with BF ‐core were designed synthesized. They displayed intramolecular charge transfer characteristics dissimilar reversible behaviors (red‐shift for blue‐shift ). Based powder X‐ray diffraction patterns quantum chemical calculation results, it was responsible behavior that reduced molecular polarity...

10.1002/slct.202303763 article EN ChemistrySelect 2024-02-21

Abstract To further explore the application of Schiff bases in latent fingerprint detection, two containing ─N═CH─ fragment at different positions on pyridine skeleton, which py‐3‐TPA with 3‐position and that locating 2‐position for py‐2‐TPA , were synthesized. Both displayed solvent‐dependent behaviors organic solvents polarities emission spectra, their solid state luminescent under a UV lamp, both could be well explained by time‐dependent density functional theory calculations,...

10.1002/slct.202500742 article EN ChemistrySelect 2025-04-27

Abstract To better understand the relationship between molecular structure and mechanofluorochromic characteristics, three carbazole‐based N^O‐chelated difluoroboron compounds ( Cz‐S‐BF 2 , Cz‐PhNp‐S‐BF Cz‐BNp‐S‐BF ) with different aryl substituents moieties were designed synthesized. The behaviours of (luminescence from bluish‐green to yellowish‐green, emission 504 535 nm) without substitution green yellow, 521 557 a phenyl‐naphthalene group underwent reversible conversion using...

10.1002/bio.4532 article EN Luminescence 2023-06-09

池可心 e ( a 昆明学院化学化工学院 云南省金属有机分子材料与器件重点实验室 昆明 650214) b 红河学院化学与资源工程学院 云南省天然药物与化学生物学重点实验室 云南蒙自 661100

10.6023/cjoc202211030 article KO Chinese Journal of Organic Chemistry 2023-01-01
Coming Soon ...