Cangjie Yang

ORCID: 0009-0007-1008-6257
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About
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Research Areas
  • Luminescence and Fluorescent Materials
  • Nanoplatforms for cancer theranostics
  • Advanced Polymer Synthesis and Characterization
  • Nanoparticle-Based Drug Delivery
  • Catalysis for Biomass Conversion
  • Silicone and Siloxane Chemistry
  • Electrocatalysts for Energy Conversion
  • Carbohydrate Chemistry and Synthesis
  • Chemical Synthesis and Analysis
  • Click Chemistry and Applications
  • Perovskite Materials and Applications
  • Dendrimers and Hyperbranched Polymers
  • Molecular Sensors and Ion Detection
  • Advanced battery technologies research
  • Porphyrin and Phthalocyanine Chemistry
  • Covalent Organic Framework Applications
  • Advanced Photocatalysis Techniques
  • biodegradable polymer synthesis and properties
  • Photochromic and Fluorescence Chemistry
  • Supramolecular Self-Assembly in Materials
  • Proteoglycans and glycosaminoglycans research
  • Machine Fault Diagnosis Techniques
  • Glycosylation and Glycoproteins Research
  • Sulfur-Based Synthesis Techniques
  • Quantum Dots Synthesis And Properties

Xiamen University
2010-2024

Boston College
2018-2023

Nanyang Technological University
2014-2022

Nanjing University of Aeronautics and Astronautics
2021

National Central University
2011

Abstract NiFe‐based layered double hydroxides (LDHs) are among the most efficient oxygen evolution reaction (OER) catalysts in alkaline medium, but their long‐term OER stabilities questionable. In this work, it is demonstrated that structure makes bulk NiFe LDH intrinsically not stable and deactivation mechanism of further revealed. Both operando electrochemical structural characterizations show interlayer basal plane contributes to activity, slow diffusion proton acceptors (e.g., OH − )...

10.1002/adma.201903909 article EN Advanced Materials 2019-08-28

ADVERTISEMENT RETURN TO ISSUEPREVViewpointNEXTUse of Platinum as the Counter Electrode to Study Activity Nonprecious Metal Catalysts for Hydrogen Evolution ReactionRong Chen†, Cangjie Yang†, Weizheng Cai†, Hsin-Yi Wang†, Jianwei Miao†, Liping Zhang†, Shengli Chen*‡, and Bin Liu*†View Author Information† School Chemical Biomedical Engineering, Nanyang Technological University, 62 Drive, Singapore 637459, Singapore‡ College Chemistry Molecular Sciences, Wuhan 430072, People’s Republic...

10.1021/acsenergylett.7b00219 article EN ACS Energy Letters 2017-04-18

The orthogonal sulfur-fluoride exchange reaction (SuFEx) and copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) are employed to synthesize sequence-regulated synthetic polymers. high efficiency broad tolerance of SuFEx CuAAC diverse chemical functionalities enable the one-pot synthesis polydispersed sequence-controlled polymers by step-growth copolymerization in yield sequence complexity. Furthermore, iterative coupling reactions on a solid support, without need protecting groups, afford...

10.1002/anie.201811051 article EN Angewandte Chemie International Edition 2018-10-16

Amphiphilic star-like block copolymers form robust biocompatible unimolecular micelles that are efficient in the delivery of anticancer drugs such as doxorubicin.

10.1039/c5cc02743h article EN Chemical Communications 2015-01-01

A facile and scalable co-precipitation method is developed to prepare stable colloidal NiFe-LDH nanoparticles at room temperature. We further scrolled into well-aligned multi-walled carbon nanotube (MWCNT) sheets form binder-free hybrid microfiber electrodes, which showed excellent OER activity, reaching 180 mA cm-2 a small overpotential of 255 mV with outstanding durability.

10.1039/c5nh00082c article EN Nanoscale Horizons 2015-12-02

Sequence-controlled polymers are an emerging class of synthetic with a regulated sequence monomers. In the past decade, tremendous progress has been made in synthesis sophisticated control approaching level manifested biopolymers. contrast, exploration novel functions that can be achieved by controlling polymer sequences represents focus science. This Viewpoint will survey recent advances functional applications sequence-controlled and provide perspective on challenges outlook for pursuing...

10.1021/acsmacrolett.0c00855 article EN ACS Macro Letters 2021-01-22

Theranostic unimolecular micelles of highly fluorescent amphiphilic conjugated bottlebrushes loaded with anticancer drugs are efficient for cancer imaging and therapy.

10.1039/c6py01838f article EN Polymer Chemistry 2016-01-01

Near-infrared (NIR) light-responsive hydrogels are important for biomedical applications, such as remote-controlled release, but the NIR agents previously used were largely limited to heavy-metal inorganic materials gold nanoparticles. In this article, we report a new type of photothermal-responsive hydrogel that can undergo structural changes in response light applications drug delivery and controlled release. The synthesized by integrating narrow-bandgap semiconductor polymer...

10.1021/acsami.7b01016 article EN ACS Applied Materials & Interfaces 2017-03-17

We report a facile and general strategy for enhancing the photostability of organic fluorophores bioimaging applications. As proof concept, bright robust fluorescence was observed in solid states well-defined synthetic polymer polycaprolactone consisting di(thiophene-2-yl)-diketopyrrolopyrrole covalently linked middle chain as biocompatible bioresorbable matrix. The nanoparticles prepared through nanoprecipitation process these polymers could be internalized by both tumor cells stem with...

10.1039/c4nr05576d article EN Nanoscale 2014-11-19

A new crystallization-induced red-emitting luminogen based on a biodegradable indigo derivative forms well-defined microcrystals in tetrahydrofuran–water mixtures upon ultrasonication.

10.1039/c4cc09540e article EN Chemical Communications 2015-01-01

Conjugated porous polymers with narrow bandgaps, tunable morphologies, porosities and optoelectronic properties are synthesized <italic>via</italic> facile direct arylation polymerization.

10.1039/c6py01453d article EN cc-by-nc Polymer Chemistry 2016-01-01

This article describes molecular design, synthesis and characterization of colloidal nanoparticles containing polycaprolactone-grafted conjugated polymers that exhibit strong far red/near-infrared (FR/NIR) fluorescence for bioimaging. Specifically, we synthesized two kinds polymer bottle brushes (PFTBout-g-PCL PFTBin-g-PCL) with different positions the hexyl groups on thiophene rings. A synthetic amphiphilic block copolymer PCL-b-POEGMA was employed as surfactants to encapsulate PFTB-g-PCL...

10.1021/acs.biomac.6b00092 article EN Biomacromolecules 2016-03-24

Colloidal nanoparticles (NPs) containing near-infrared-fluorescent J-aggregates (JAGGs) of pyrrolopyrrole cyanines (PPcys) stabilized by amphiphilic block co-polymers were prepared in aqueous medium. JAGG formation can be tuned means the chemical structure PPcys, concentration chromophores inside polymeric NPs, and ultrasonication. The NPs exhibit a narrow emission band at 773 nm, fluorescence quantum yield comparable to that indocyanine green, significantly enhanced photostability, which is...

10.1002/chem.201604741 article EN Chemistry - A European Journal 2016-12-05

Triazine-based conjugated porous polymers were synthesised by direct arylation polymerization and used as photocatalysts for aerobic oxidation of benzylamine.

10.1039/c8py00025e article EN Polymer Chemistry 2018-01-01

Direct arylation polycondensation enables efficient synthesis of narrow-bandgap, well-defined alternating D–A copolymers consisting naphthalene diimide as the acceptor unit.

10.1039/c5py00595g article EN Polymer Chemistry 2015-01-01

Multifunctional stable and stimuli-responsive drug delivery systems are important for efficient cancer treatment due to their advantages such as enhanced cancer-targeting efficiency, improved pharmacokinetics, minimized leaching, reduced undesirable side effects. Here we report a robust pH-responsive anticancer system based on unimolecular micelles of star-like amphiphilic copolymers. The polymers (denoted CPOFs) were facilely synthesized via one-step atom transfer radical polymerization...

10.1021/acs.molpharmaceut.6b00708 article EN Molecular Pharmaceutics 2016-09-29

Abstract O‐sulfation is an important chemical code widely existing in bioactive molecules, but the scalable and facile synthesis of complex molecules carrying O‐sulfates remains challenging. Reported here a general approach to by sulfur(VI) fluoride exchange (SuFEx) reaction between aryl fluorosulfates silylated hydroxy groups. Efficient sulfate diester formation was achieved through systematic optimization electronic properties fluorosulfates. The versatility this strategy demonstrated...

10.1002/anie.202007211 article EN Angewandte Chemie International Edition 2020-07-09

As an inedible component of biomass, lignin features rich functional groups that are desired for chemical syntheses. How to effectively depolymerize without compromising the more valuable cellulose and hemicellulose has been a significant challenge. Existing biomass processing procedures either induce extensive condensation in greatly hinders its utilization or focus on fully depolymerizing produce monomers difficult separate subsequent synthesis. Here, we report new approach selective...

10.1021/acscentsci.2c01257 article EN cc-by ACS Central Science 2022-12-28

Abstract The orthogonal sulfur–fluoride exchange reaction (SuFEx) and copper(I)‐catalyzed azide–alkyne cycloaddition (CuAAC) are employed to synthesize sequence‐regulated synthetic polymers. high efficiency broad tolerance of SuFEx CuAAC diverse chemical functionalities enable the one‐pot synthesis polydispersed sequence‐controlled polymers by step‐growth copolymerization in yield sequence complexity. Furthermore, iterative coupling reactions on a solid support, without need protecting...

10.1002/ange.201811051 article EN Angewandte Chemie 2018-10-16

Conjugated microporous polymers are synthesized <italic>via</italic> facile direct arylation polymerization, resulting in conjugated networks with hierarchical porosity and a narrow bandgap of 1.5 eV.

10.1039/c6py00719h article EN Polymer Chemistry 2016-01-01
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