Senbin Chen

ORCID: 0000-0001-5599-6819
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Research Areas
  • Supramolecular Self-Assembly in Materials
  • Advanced Polymer Synthesis and Characterization
  • Polymer composites and self-healing
  • Nanoplatforms for cancer theranostics
  • Dendrimers and Hyperbranched Polymers
  • Supramolecular Chemistry and Complexes
  • Metal-Organic Frameworks: Synthesis and Applications
  • Pickering emulsions and particle stabilization
  • Block Copolymer Self-Assembly
  • Polydiacetylene-based materials and applications
  • Polymer Surface Interaction Studies
  • Luminescence and Fluorescent Materials
  • Nanoparticle-Based Drug Delivery
  • Chemical Synthesis and Analysis
  • Ionic liquids properties and applications
  • Surfactants and Colloidal Systems
  • Silicone and Siloxane Chemistry
  • Conducting polymers and applications
  • Liquid Crystal Research Advancements
  • Gold and Silver Nanoparticles Synthesis and Applications
  • Synthesis and properties of polymers
  • Photodynamic Therapy Research Studies
  • Advanced Nanomaterials in Catalysis
  • Synthetic Organic Chemistry Methods
  • Electrospun Nanofibers in Biomedical Applications

Huazhong University of Science and Technology
2018-2025

Materials Processing (United States)
2021-2022

Centre National de la Recherche Scientifique
2010-2020

Institut National des Sciences Appliquées de Lyon
2010-2020

Université Claude Bernard Lyon 1
2010-2020

Ministry of Education
2019

Martin Luther University Halle-Wittenberg
2014-2018

Luther University
2017-2018

Lanzhou University
2007-2014

Institute of Macromolecular Chemistry
2014

Integrating self-healing capability into supramolecular architectures is an interesting strategy, and can considerably enhance the performance broaden scope of applications for this important class polymers. Herein we report rational design novel V-shaped barbiturate (Ba) functionalized soft-hard-soft triblock copolymers with a reversible healing motif in central part hard block, which undergoes autonomic repair at 30 °C. The designed synthesis also offers suitable macromolecular building...

10.1002/anie.201504136 article EN Angewandte Chemie International Edition 2015-07-01

Hydrogen bonds (H-bonds) constitute highly relevant structural units of molecular self-assembly. They bridge biological and synthetic sciences, implementing dynamic properties into materials molecules, not achieved via purely covalent bonds. Phase segregation on the other hand represents another important assembly principle, responsible for, e.g., cell compartimentation, membrane-formation, microphase in polymers. Yet, despite expanding elegant strategies supramolecular polymers,...

10.1021/acs.accounts.6b00174 article EN Accounts of Chemical Research 2016-06-17

Abstract High‐performance adhesives are of great interest in view industrial demand. We herein identify a straightforward synthetic strategy towards universal hydrogen‐bonded (H‐bonded) polymeric adhesives, using side‐chain barbiturate (Ba) and Hamilton wedge (HW) functionalized copolymer. Starting from rubbery copolymer containing thiolactone derivatives, Ba HW moieties tethered as pendant groups via an efficient one‐pot two‐step amine‐thiol‐bromo conjugation. Hetero‐complementary Ba/HW...

10.1002/anie.202203876 article EN Angewandte Chemie International Edition 2022-04-15

Adhesive bonding to diverse substances is vital a great number of the established, cutting-edge and emerging applications. We have witnessed, in last few years, transformative progress achieving robust adhesive tunable debonding behavior, which mostly employing supramolecular forces. Among forces, contribution hydrogen-bonds (H-bonds) adhesives, on modality directionality, selectivity sensitivity, can function as nano-scaled agents for improved interfacial interactions, thus paved novel...

10.1016/j.supmat.2023.100032 article EN cc-by-nc-nd Supramolecular Materials 2023-02-10

The outcomes of combined cancer therapy are largely related to loading content and contribution each therapeutic agent; however, fine-tuning the ratio two coloaded components toward precise is a great challenge still remains in its infancy. We herein develop supramolecular polymer scaffold optimize coloading chemotherapeutic agent photosensitizer through hydrogen-bonding (H-bonding) interaction, for maximizing efficacy intelligent chemo/photodynamic therapies (CT/PDT). To do so, we first...

10.1021/acsnano.3c08359 article EN ACS Nano 2024-01-08

Abstract The structural rigidity of thiourea (TU) motifs has made them useful in supramolecular (bio)materials. However, the role TU motif a single system endowing dual noncovalent interactions, i.e., Hydrogen‐bonding (H‐bonding) association and metal‐coordination interaction, to afford nanomedicine is still unexplored. Herein smart polymeric constructed via privileged toward synergistic chemo/chemodynamic (CT/CDT) cancer therapy reported. study first synthesized six‐arm star‐shaped...

10.1002/adfm.202400113 article EN Advanced Functional Materials 2024-04-03

Photonic crystals (PCs) are ideal candidates for reflective color pigments with high purity and brightness due to tunable optical stop band. Herein, the generation of PC microspheres through 3D confined supramolecular assembly block copolymers (polystyrene-block-poly(2-vinylpyridine), PS-b-P2VP) small molecules (3-n-pentadecylphenol, PDP) in emulsion droplets is demonstrated. The intrinsic structural colors effectively regulated by tuning hydrogen-bonding interaction between P2VP blocks PDP,...

10.1002/smll.202001315 article EN Small 2020-06-22

Abstract Precise cancer nanomedicine requires rational molecular instructions of therapeutic agents. Harnessing the structure‐property‐function relationships represents a practical strategy toward smart and effective nanomedicine. A structurally novel hydrogen‐bonded (H‐bonded) supramolecular nanoformulation generated by orthogonal self‐sorting assembly chemo‐prodrug (FPtF) phototherapeutics (BPeB) is here reported, to reach an autonomous with improved anti‐tumor efficacy combining...

10.1002/adma.202502416 article EN Advanced Materials 2025-04-07

Supramolecular miktoarm stars (AB2 type) composed of poly (methyl methacrylate)-polystyrene2 (PMMA-PS2), poly(isoprene)-polystyrene2 (PI-PS2), and poly(vinyl acetate)-polystyrene2 (PVAc-PS2) were successfully synthesized by assembling reversible addition−fragmentation chain transfer (RAFT)-polymerized chains bearing hydrogen-bonding heterocomplementary associating units. To this end, thymine diaminopyridine-functionalized agents designed to efficiently mediate the polymerization vinyl...

10.1021/ma101044y article EN Macromolecules 2010-07-02

We report an original strategy toward the straightforward preparation of precisely defined telechelic H-bonding polymers and generation supramolecular block copolymers thereof. Making use α,ω-functionalized symmetrical trithiocarbonate bearing thymine groups at both chain ends, a series heterocomplementary were effortlessly generated by RAFT polymerization in one step process. The resulting macromolecules selectively interacted with α-DAP-functionalized chains to afford solution bulk. These...

10.1021/ma200540u article EN Macromolecules 2011-04-29

Tumor recurrence and metastasis are the main causes of cancer mortality; traditional chemotherapeutic drugs have severe toxicity side effects in treatment. To overcome these issues, here, we present a pH-responsive, self-destructive intelligent nanoplatform for magnetic resonance/fluorescence dual-mode image-guided mitochondrial membrane potential damage (MMPD)/photodynamic (PDT)/photothermal (PTT)/immunotherapy breast treatment with external near infrared (NIR) light irradiation. do so,...

10.1021/acsami.2c22338 article EN ACS Applied Materials & Interfaces 2023-02-08

The field of anticancer nanomedicine seeks to boost the arsenal's exploitation with intelligent performance. One opportunistic choice comes from fabrication amphiphilic polymer micelles that are reversibly crosslinked. Here, hydrogen-bond (H-bond)-driven core-crosslinked supramolecular (FUS/ICG@PEDD) constructed, co-loading α,ω-functionalized symmetrical H-bonding prodrug 5-fluorouracil-acetic acid–SS–5-fluorouracil-acetic acid (FUS) and a dual photothermal/photodynamic agent (indocyanine...

10.1021/acs.chemmater.3c01375 article EN Chemistry of Materials 2023-09-04

One of the major goals biomedical science is to pioneer advanced strategies toward precise and smart medicine. Hydrogen-bonding (H-bonding) assembly incorporated with an aggregation-induced emission (AIE) capability can serve as a powerful tool for developing supramolecular nanomedicine clear tumor imaging therapeutic performance. We here report H-bonded polymeric nanoformulation AIE characteristic antitumor therapy. To do so, we first design structurally novel tetraphenylethylene...

10.1021/acsmacrolett.3c00493 article EN ACS Macro Letters 2023-09-28

In this work, it is reported that large-area (centimeter-scale) arrays of non-close-packed polystyrene-tethered gold nanorod (AuNR@PS) can be prepared through a liquid-liquid interfacial assembly method. Most importantly, the orientation AuNRs in controlled by changing intensity and direction electric field applied solvent annealing process. The interparticle distance AuNR tuned varying length polymer ligands. Moreover, AuNR@PS with short PS ligand are favorited to form orientated assistance...

10.1002/smll.202208288 article EN Small 2023-03-06

Heterotelechelic poly(n-butyl acrylate)s (PnBuA) bearing two different and complementing supramolecular groups (namely, barbiturate (Ba) the Hamilton wedge (HW)) at their α-end ω-end (Ba–PnBuA–HW) were prepared by a combination of reversible addition–fragmentation chain transfer (RAFT) process thio–bromo click reaction. The successful synthesis heterotelechelic H-bonding polymer Ba–PnBuA–HW (Mn,NMR = 7700 g/mol, Mn,SEC 7500 PDI 1.25) was proven 1H NMR MALDI-TOF mass spectrometry....

10.1021/mz500747t article EN ACS Macro Letters 2014-12-22

Complete cancer cure and healing are still difficult, owing to its complexity heterogeneity. Integration of supramolecular forces, for example, hydrogen bonds (H-bonds), anti-cancer nanomedicine affords new scaffolds biomedical material decoration, featuring the advantages dynamic property easier processability. Here, we target construction H-bond-mediated polymer micelles, loaded with a chemotherapeutic drug along photothermal agent synergistic chemo-/photothermal therapies (CT/PTT). To do...

10.1021/acs.biomac.2c00717 article EN Biomacromolecules 2022-09-08

Abstract Adhesive conducting elastomers are rising materials towards cutting‐edge applications in wearable and implantable soft electronics. Yet, engineering the conductive adhesives with robust tunable interfacial bonding strength is still its infancy stage. We herein identify a structurally novel supramolecular polymer scaffold, characterized by synergistic coexistence of hydrogen‐bonding (H−bonding) interactions electrostatic ionic junctions, endowing elastic remarkable...

10.1002/anie.202415386 article EN Angewandte Chemie International Edition 2024-10-25

A novel dextran-SG1 macro-alkoxyamine was designed to afford amphiphilic linear block copolymers synthesized by nitroxide mediated polymerization toward the formation of hierarchically structured bio-resourced honeycomb films.

10.1039/c4py00390j article EN Polymer Chemistry 2014-01-01

Abstract Integrating self‐healing capability into supramolecular architectures is an interesting strategy, and can considerably enhance the performance broaden scope of applications for this important class polymers. Herein we report rational design novel V‐shaped barbiturate (Ba) functionalized soft–hard–soft triblock copolymers with a reversible healing motif in central part hard block, which undergoes autonomic repair at 30 °C. The designed synthesis also offers suitable macromolecular...

10.1002/ange.201504136 article EN Angewandte Chemie 2015-07-01

The facile preparation of novel supramolecular (ABAC)<sub>n</sub> multiblock copolymers from Hamilton wedge and barbiturate functionalized H-bonding RAFT agents is reported.

10.1039/c3py01482g article EN Polymer Chemistry 2014-01-01
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