Xiaobo Huang

ORCID: 0000-0002-4876-8372
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About
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Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Luminescence and Fluorescent Materials
  • Molecular Sensors and Ion Detection
  • Microbial infections and disease research
  • Catalytic C–H Functionalization Methods
  • Bacteriophages and microbial interactions
  • Animal Virus Infections Studies
  • Organic Light-Emitting Diodes Research
  • Aquaculture disease management and microbiota
  • Sulfur-Based Synthesis Techniques
  • Ecology and Vegetation Dynamics Studies
  • Crystallography and molecular interactions
  • Viral gastroenteritis research and epidemiology
  • Virus-based gene therapy research
  • Organoselenium and organotellurium chemistry
  • Fungal Plant Pathogen Control
  • Polydiacetylene-based materials and applications
  • Supramolecular Chemistry and Complexes
  • Porphyrin and Phthalocyanine Chemistry
  • Conducting polymers and applications
  • Viral Infections and Immunology Research
  • Nanoplatforms for cancer theranostics
  • Quinazolinone synthesis and applications
  • Supramolecular Self-Assembly in Materials

Ministry of Education of the People's Republic of China
2025

Sichuan Agricultural University
2016-2025

Wenzhou University
2016-2025

Henan University of Science and Technology
2021-2025

Chinese Academy of Forestry
2015-2024

University of Applied Sciences and Arts of Southern Switzerland
2024

China Southern Power Grid (China)
2024

Ningxia Medical University
2023-2024

AGH University of Krakow
2024

North China University of Water Resources and Electric Power
2022-2024

Research on materials with pure organic room temperature phosphorescence (RTP) and their application as single-molecule white light emitters is a hot area relies the design of highly efficient RTP luminogens. Herein, facile strategy heavy-atom-participated anion-π+ interactions proposed to construct RTP-active salt compounds (1,2,3,4-tetraphenyloxazoliums different counterions). Those heavy-atom counterions (bromide iodide ions) exhibit outstanding due external heavy atom effect via...

10.1038/s41467-018-05298-y article EN cc-by Nature Communications 2018-07-23

Abstract Organic near-infrared room temperature phosphorescence materials have unparalleled advantages in bioimaging due to their excellent penetrability. However, limited by the energy gap law, (>650 nm) are very rare, moreover, lifetimes of these short. In this work, we obtained organic with long wavelengths (600/657–681/732 and (102–324 ms) for first time through guest-host doped strategy. The guest molecule has sufficient conjugation reduce lowest triplet level host assists exciton...

10.1038/s41467-021-27914-0 article EN cc-by Nature Communications 2022-01-10

Recent years have witnessed the significant role of anion-π+ interactions in many areas, which potentially brings opportunity for development aggregation-induced emission (AIE) systems. Here, a new strategy that utilized to block detrimental π-π stacking was first proposed develop inherent-charged AIE Two AIE-active luminogens, namely, 1,2,3,4-tetraphenyloxazolium (TPO-P) and 2,3,5-triphenyloxazolium (TriPO-PN), were successfully synthesized. Comprehensive techniques such as single-crystal...

10.1021/jacs.7b10150 article EN Journal of the American Chemical Society 2017-10-30

A series of organic host–guest materials with multifunctional luminescence were constructed. Four isoquinoline derivatives used as the guests, and benzophenone was host. The doped system exhibited excellent dual emission cyan fluorescence orange-yellow room-temperature phosphorescence, could be combined into almost pure white-light emission. Importantly, relative intensity fluorescence–phosphorescence adjusted by changing excitation wavelength, phosphorescence being significantly higher than...

10.1021/acs.jpclett.1c00188 article EN The Journal of Physical Chemistry Letters 2021-02-12

Abstract A strategy is pioneered for achieving high-temperature phosphorescence using planar rigid molecules as guests and polymers host matrix. The configuration can resist the thermal vibration of guest at high temperatures, rigidity matrix further enhances resistance guest. doped materials exhibit an afterglow 40 s 293 K, 20 373 6 413 a 1 433 K. experimental results indicate that rotational ability groups connected to gradually increases, performance decreases. In addition, utilizing...

10.1038/s41467-024-45678-1 article EN cc-by Nature Communications 2024-02-10

In this perspective, the progress in ion-regulated organic RTP materials and described roles of ions, including ion–π interactions, electrostatic coordinate have been summarized.

10.1039/d3sc06931a article EN cc-by-nc Chemical Science 2024-01-01

The review focuses on the influence of some important factors generation new and/or high contrast mechanofluorochromic-active organic compounds by structural modifications traditional fluorophores.

10.1039/c8tc00043c article EN Journal of Materials Chemistry C 2018-01-01

The first example of a copper-catalyzed cascade reaction (2-aminophenyl)methanols with aldehydes using the combination cerium nitrate hexahydrate and ammonium chloride has been developed, leading to wide range 2-substituted quinazolines in moderate excellent yields. efficiency this transformation was demonstrated by compatibility functional groups. Thus, method represents convenient practical strategy for synthesis quinazoline derivatives.

10.1021/jo401908g article EN The Journal of Organic Chemistry 2013-10-17

A new and efficient copper-catalyzed C3 aryl- heteroarylselenation of indoles employing selenium powder has been developed. The advantages this chemistry involve the use cheap selenating reagents, tolerance a variety functional groups, practicality. In addition, protocol further elaborated in an intramolecular phenylselenation (hetero) aryl C–H bond to construct important motif benzoselenopheno[3,2-b]indole. preliminary mechanism study suggests that reaction starts with Ullman-type...

10.1021/acs.joc.6b00229 article EN The Journal of Organic Chemistry 2016-05-18

We first report several bright solid-state red-emissive BODIPYs with high fluorescence quantum yields for unusual high-contrast mechanohypsochromism.

10.1039/c8tc06421k article EN Journal of Materials Chemistry C 2019-01-01

A series of dicyanomethylene-1,4-dihydropyridine (DCMP) derivatives with aggregation-induced emission (AIE) were designed and synthesized. These target compounds emit low fluorescence in THF solutions because the free rotation phenyl dihydropyridine rings about axes olefinic double bonds resultant nonradiative decay process, but they exhibit strong aggregate state restriction intramolecular (RIR), as confirmed by solution thickening cooling experiments. Compared almost-planar...

10.1021/jp511060k article EN The Journal of Physical Chemistry C 2015-03-06

Presented in this work is a novel methodology for the synthesis of selenated benzofurans (or benzothiophenes) via AgNO2-catalyzed radical cyclization 2-alkynylanisoles 2-alkynylthioanisoles), Se powder, and arylboronic acids. This method enables construction benzofuran (benzothiophene) ring, two C–Se bonds, C–O(S) bond as well cleavage single step. Preliminary mechanistic studies imply that proceeds an aryl selenium intermediate.

10.1021/acs.orglett.9b02315 article EN Organic Letters 2019-08-13

A doped system with strong pure phosphorescent emission has been constructed, and the QY phos. can reach up to 64%. The ISC efficiency of excitons be adjusted by changing excitation wavelength, so materials selectively emit green phosphorescence or cyan fluorescence.

10.1039/d1tc00403d article EN Journal of Materials Chemistry C 2021-01-01

An anthracene unit was successfully fused to the zigzag edge of a boron dipyrromethene (BODIPY) core by an FeCl(3)-mediated oxidative cyclodehydrogenation reaction. Meanwhile, dimer also formed both intramolecular cyclization and intermolecular coupling. The anthracene-fused BODIPY monomer 7a 7b showed small energy gaps (∼1.4 eV) near-infrared absorption/emission. Moreover, they exhibited high photostability.

10.1021/ol202493c article EN Organic Letters 2011-10-20

Copper-catalyzed direct C–H arylation of pyridine<italic>N</italic>-oxides with arylboronic esters for the one-pot synthesis 2-arylpyridines without an additional reductant.

10.1039/c3cc48767a article EN Chemical Communications 2014-01-01

Despite the great potential of heteroatom-containing polycyclic aromatic hydrocarbons in organic optoelectronics, there are very limited reports on heteroaromatics containing a B-N-B bond π-scaffold. Herein, stable 1,9-dibora-9a-azaphenalenyl (DBAP) derivatives, named BNB-embedded phenalenyls, presented. The DBAP skeleton contains three-center two-π-electron moiety with 12 π-electrons and can be regarded as isoelectronic structure phenalenyl cation. Chemical reduction phenyl derivative by...

10.1021/jacs.7b07375 article EN Journal of the American Chemical Society 2017-10-13

Three donor (D)-π-acceptor (πA) indene-1,3-dionemethylene-1,4-dihydropyridine (IDM-DHP) derivatives with triphenylamine (TPA)/bis(diphenylamino)triphenylamine (BDPA-TPA) end groups were designed and synthesized. These target compounds highly twisted conformations showed aggregation-induced emission enhancement properties in their THF/water mixtures due to the restriction of intramolecular rotation, distinct piezofluorochromic (PFC) solid state. Interestingly, solvent-induced changes similar...

10.1021/acs.jpcc.5b06432 article EN The Journal of Physical Chemistry C 2015-09-18
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