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Jacky Wing Yip Lam

Researcher at Hong Kong University of Science and Technology

Publications -  698
Citations -  55632

Jacky Wing Yip Lam is an academic researcher from Hong Kong University of Science and Technology. The author has contributed to research in topics: Polymer & Polymerization. The author has an hindex of 106, co-authored 619 publications receiving 44048 citations. Previous affiliations of Jacky Wing Yip Lam include University of Hong Kong & Shenzhen University.

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Exploration of Effective Catalysts for Diyne Polycyclotrimerization, Synthesis of an Ester-Functionalized Hyperbranched Polyphenylene, and Demonstration of Its Utility as a Molecular Container with Implication for Controlled Drug Delivery

TL;DR: In this paper, the first examples of a group of effective ruthenium catalysts for polycyclotrimerization were presented, where the polymerization reactions of an arylene bipropiolate monomer initiated by the Ru(II−IV) complexes of CpRu(PPh3)2Cl, Cp*RuCl2]n, and [Ru(η 3:η3-C10H16)(μ-Cl)Cl]2 (Cp = cyclopentadienyl, cp* = pent
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Structural features and optical properties of a carbazole-containing ethene as a highly emissive organic solid

TL;DR: In this paper, a carbazole derivative with aggregation-induced emission characteristics was constructed to suppress the luminescence quenching effect in the condensed phase, and the highly blue emissive crystal fibers exhibit optical waveguide properties.
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Functional isocoumarin-containing polymers synthesized by rhodium-catalyzed oxidative polycoupling of aryl diacid and internal diyne

TL;DR: In this paper, an atom-economical and straightforward polymerization method to generate functional isocoumarin-containing polymers was developed, which achieved high thermal stability, optical transparency and film-forming ability.
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Ratiometric Detection of Mitochondrial Thiol with a Two-Photon Active AIEgen

TL;DR: A ratiometric aggregation-induced emission luminogen (AIEgen) called TPE-PBP for thiol detection was developed by introducing a para-dinitrophenoxy benzylpyridinium moiety to tetraphenylethylene, exhibiting excellent biocompatibility, high photostability, and large two-photon absorption cross-section.
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Naphthalene-substituted 2,3,4,5-tetraphenylsiloles: synthesis, structure, aggregation-induced emission and efficient electroluminescence

TL;DR: Two thermally stable naphthalene-substituted 2,3,4,5tetraphenylsiloles, 1,1-dimethyl-2,5-bis[4-(naphthalen-1-yl)phenyl]-3, 4-diphenyl-silole (D- 1-NpTPS) and 1, 1-dimyl-2.5-bi[4.4]-3.4-diminylsilole(D-2-Npsilole) have been synthesized and