Shrong-Shi Lin
Peking University
15 Papers
228 Citations
Shrong-Shi Lin is an academic researcher from Peking University. The author has contributed to research in topics: Aqueous solution & Dynamic light scattering. The author has an hindex of 8, co-authored 15 publications. Previous affiliations of Shrong-Shi Lin include University at Buffalo.
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Papers
Acid-Sensitive Polymeric Micelles Based on Thermoresponsive Block Copolymers with Pendent Cyclic Orthoester Groups
Xiaonan Huang,Fu-Sheng Du,Jing Cheng,Yong-Quan Dong,Dehai Liang,Shou-Ping Ji,Shrong-Shi Lin,Zi-Chen Li +7 more
TL;DR: An orthoester-containing monomer, trans-N-(2-ethoxy-1,3-dioxan-5-yl)acrylamide (tNEA), was synthesized as mentioned in this paper.
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Covalently Bound Organic Silicate Aluminum Hybrid Coagulants: Preparation, Characterization, and Coagulation Behavior
TL;DR: The hybrid coagulant with APDES as the silicon source exhibited the best coagulation behavior in terms of HA removal and turbidity removal, due to the combination of the zeta potential, Al species distribution, and organic functional groups.
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Stereochemical Effect of Trans/Cis Isomers on the Aqueous Solution Properties of Acid-Labile Thermoresponsive Polymers
TL;DR: In this article, two acid-labile, thermoresponsive poly(methacrylamide)s with the pendant cyclic orthoester moieties of trans and cis configurations, PtNEM and PcNEM, were synthesized via free radical polymerization of the corresponding trans-and cis isomers of N-(2-ethoxy-1,3-dioxan-5-yl)methACrylamides (NEM).
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Aqueous Solution Properties of the Acid-Labile Thermoresponsive Poly(meth)acrylamides with Pendent Cyclic Orthoester Groups
TL;DR: A series of poly(meth)acrylamide derivatives with pendent six-member cyclic orthoester groups, i.e., poly(N-(2-alkyloxy-1,3-dioxan-5-yl)methacryamide)s and poly(n-(N-(n)-acetyloxy 1,3)-dioxane 5-yl poly(poly(n)-acrylonitrivanic acid)s, have been synthesized and characterized as mentioned in this paper.
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The design, synthesis, and biological evaluation of novel substituted purines as HIV-1 Tat-TAR inhibitors.
TL;DR: A series of novel substituted purines containing a side chain with a terminal amino or guanidyl group were designed and synthesized as HIV-1 Tat-TAR inhibitors and suggest that the compounds bind to TAR RNA in two different modes.
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