We investigate a minimal equilibrium polymerization model for the competition between self-assembly on a boundary and in solution that arises when an assembling system is in the presence of an adsorbing interface. Adsorption generally occurs upon cooling, but assembly (equilibrium polymerization) may arise either upon cooling or heating. Both cases are shown to exhibit a coupling between adsorption and self-assembly. When both assembly and adsorption proceed upon cooling, a change in the ratio of the enthalpy of adsorption to the enthalpy of assembly in solution can switch the system between a predominance of self-assembly in solution to assembly on the substrate. If assembly is promoted by heating and adsorption by cooling, as in many self-assembling proteins in aqueous solution, then a self-assembly analog of a closed loop phase boundary is found. In particular, the order parameter for assembly on the surface exhibits a peak as a function of temperature. As demonstrated by illustrative examples, the coupling between surface adsorption and self-assembly provides a powerful means of switching self-assembly processes on and off. Understanding and controlling this switching phenomenon will be useful in designing and directing self-assembly processes on surfaces for applications to nanomanufacturing and in developing treatments for diseases arising from pathological adsorption-induced assembly.
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http://dx.doi.org/10.1063/1.3077866 | DOI Listing |
J Colloid Interface Sci
December 2024
Key Laboratory of Green Utilization of Critical Non-metallic Mineral Resources of Ministry of Education, Wuhan University of Technology, Wuhan, Hubei 430073, China; School of Resources and Environmental Engineering, Wuhan University of Technology, Wuhan, Hubei 430073, China. Electronic address:
Development of efficient and stable bifunctional transition metal phosphide catalysts is critical for advancing hydrogen production technologies. Herein, RuCo co-doped NiP (RuCoNiP) was designed and synthesized by one-step electrodeposition for Ni electronic structure modulation, and evolved to RuCoNiP@α-Ni(OH) and RuCoNiP@Co/Ni(OH) heterointerfaces by self-assembled reconstruction during HER and OER processes, respectively. RuCoNiP@α-Ni(OH) enhances HER activity (305.
View Article and Find Full Text PDFInorg Chem
December 2024
Departament de Química, Universitat de les Illes Balears, Ctra Valldemossa, Km 7.5., 07122 Palma de Mallorca, Spain.
Metalloporphyrins have been widely utilized as building blocks for molecular self-assembly in organic solvents, but their application in water is less common due to competition from water molecules for the metal center. However, Co(III) metalloporphyrins are notable for their strong binding to two aromatic amine ligands in aqueous buffers. In this study, we present a comprehensive investigation of the binding behavior of Co(III) tetraphenyl sulfonic acid porphyrin with selected aromatic and aliphatic amines in aqueous solution.
View Article and Find Full Text PDFAdv Mater
December 2024
College of Chemistry, State Key Laboratory of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, Nankai University, Tianjin, 300071, P. R. China.
Chem Sci
December 2024
Department of Chemistry, Gyeongsang National University Jinju 52828 Korea
Understanding the pathway complexity of supramolecular polymerization in biomimetic systems has been a challenging issue due to its importance in the development of rationally controlled materials and insight into self-assembly in nature. We herein report a kinetic trapping strategy as a new methodology on how to control the pathway of metallosupramolecular polymerization by employing secondary metal ions and/or ligands which form competitive complex species. For this, we proposed monoalkynylplatinum(ii) metalloligand (Pt-L) derived from a bis(amideterpyridine) receptor with one unoccupied terpyridyl terminal as a coordination site for the secondary metal ion (Ag or Fe).
View Article and Find Full Text PDFAdv Sci (Weinh)
November 2024
Joint Laboratory of Opto-Functional Theranostics in Medicine and Chemistry, Institute of Translational Medicine, The First Hospital of Jilin University, Changchun, 130021, P. R. China.
Phosphate and phosphonate drugs are vital in building organisms, regulating physiological processes, and exhibiting diverse biological activities, including antiviral, antibacterial, antineoplastic, and enzyme-inhibitory effects. However, their therapeutic potential is limited by the lack of advanced nanoengineering technologies. Herein, a competitive coordination strategy for nanoengineering phosphate/phosphonate drugs is introduced.
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