Green synthesis of sulfur-containing polymers by carbon disulfide-based spontaneous multicomponent polymerization

Chen, Xu; Qin, Anjun; Tang, Ben Zhong

doi:10.1039/d3gc02415f

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2024

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Cited by 4 publications

(1 citation statement)

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“…6,22–25 Up to now, only very limited MCP methodologies based on CS 2 have been reported for the preparation of sulfur-containing polymers. 26–30 Therefore, it is of great importance to develop facile and efficient MCPs to achieve various novel sulfur-containing polymers from the readily available CS 2 monomer.…”

Section: Introductionmentioning

confidence: 99%

CS₂-based one-pot multicomponent tandem polymerization toward functional polybenzothiazoles

Liu,

Zhang,

Zhang

et al. 2024

Polym. Chem.

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Section: Introductionmentioning

confidence: 99%

CS₂-based one-pot multicomponent tandem polymerization toward functional polybenzothiazoles

Liu,

Zhang,

Zhang

et al. 2024

Polym. Chem.

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Green conversion of carbon disulfide to degradable polydithiourethanes through catalyst-free multicomponent polymerizations of diamines, carbon disulfide and diacrylates

Zhao,

Wang,

Feng

et al. 2024

European Polymer Journal

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Nanomedicines with Versatile GSH-Responsive Linkers for Cancer Theranostics

Ding,

Zhou,

2024

ACS Biomater. Sci. Eng.

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Glutathione (GSH)-responsive nanomedicines have generated significant interest in biochemistry, oncology, and material sciences due to their diverse applications, including chemical and biological sensors, diagnostics, and drug delivery systems. The effectiveness of these smart GSH-responsive nanomedicines depends critically on the choice of GSH-responsive linkers. Despite their crucial role, comprehensive reviews of GSH-responsive linkers are scarce, revealing a gap in the current literature. This review addresses this gap by systematically summarizing various GSH-responsive linkers and exploring their potential applications in cancer treatment. We provide an overview of the mechanisms of action of these linkers and their bioapplications, evaluating their advantages and limitations. The insights presented aim to guide the development of advanced GSH-responsive agents for cancer diagnosis and therapy.

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Green synthesis of sulfur-containing polymers by carbon disulfide-based spontaneous multicomponent polymerization

Abstract: A spontaneous multi-component polymerization of activated internal alkynes, amines, and CS2 was established. Similar to the ancient “tenon and mortise” structure, CS2 acts as a “wedge” to link the other two monomers to form sulfur-containing polymers.

Cited by 4 publications

References 67 publications

CS₂-based one-pot multicomponent tandem polymerization toward functional polybenzothiazoles

CS₂-based one-pot multicomponent tandem polymerization toward functional polybenzothiazoles

Green conversion of carbon disulfide to degradable polydithiourethanes through catalyst-free multicomponent polymerizations of diamines, carbon disulfide and diacrylates

Nanomedicines with Versatile GSH-Responsive Linkers for Cancer Theranostics

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Green synthesis of sulfur-containing polymers by carbon disulfide-based spontaneous multicomponent polymerization

Abstract: A spontaneous multi-component polymerization of activated internal alkynes, amines, and CS2 was established. Similar to the ancient “tenon and mortise” structure, CS2 acts as a “wedge” to link the other two monomers to form sulfur-containing polymers.

Cited by 4 publications

References 67 publications

CS2-based one-pot multicomponent tandem polymerization toward functional polybenzothiazoles

CS2-based one-pot multicomponent tandem polymerization toward functional polybenzothiazoles

Green conversion of carbon disulfide to degradable polydithiourethanes through catalyst-free multicomponent polymerizations of diamines, carbon disulfide and diacrylates

Nanomedicines with Versatile GSH-Responsive Linkers for Cancer Theranostics

Contact Info

Product

Resources

About

CS₂-based one-pot multicomponent tandem polymerization toward functional polybenzothiazoles

CS₂-based one-pot multicomponent tandem polymerization toward functional polybenzothiazoles