This paper focuses on the formation of high-density, low-defect monolayers of triphosphasumanene trisulfides, which are newly synthesized electronic and geometric Janus-type molecules, in a flat-on conformation. Although the molecules stack easily because of the developed π-conjugated plane, their application as a metal coating in a flat-on conformation via an interfacial molecular film enables the work function to be tuned. Surface pressure-area isotherms of the triphosphasumanene trisulfides show a two-dimensional phase transition at the air/water interface. Atomic force microscopy observations of the transferred monolayer and in- and out-of-plane X-ray diffraction patterns of the corresponding multilayers reveal that this phase transition occurs from the flat-on to the end-on conformation. The X-ray diffraction patterns obtained in the two directions completely reversed before and after the phase transition, indicating that the molecular arrangement that is generated by layers of molecular films and resultant molecular stacking is similar. The flat-on conformation of the molecules was evident from the out-of-plane X-ray diffraction and polarized infrared spectroscopy results, which indicate that a large, low-defect monomolecular film is obtained using a toluene solution with a small diffusion coefficient. The spectroscopic results reveal triphosphasumanene trisulfide aggregation in the organized molecular film, suggesting high-density molecular packing.
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http://dx.doi.org/10.1021/acs.langmuir.9b00598 | DOI Listing |
ACS Appl Mater Interfaces
December 2024
Biological Physics Group, School of Physics and Astronomy, Faculty of Science and Engineering, The University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
Investigating the molecular conformations of monoclonal antibodies (mAbs) adsorbed at the solid/liquid interface is crucial for understanding mAb solution stability and advancing the development of mAb-based biosensors. This study examines the pH-dependent conformational plasticity of a human IgG1k mAb, COE-3, at the SiO/water interface under varying pH conditions (pH 5.5 and 9).
View Article and Find Full Text PDFAnal Chim Acta
April 2023
Department of Chemical and Materials Engineering, Concordia University, 1435 Rue Guy, S-GM 900-13, Montréal, Québec, H3H 2L5, Canada. Electronic address:
Analyzing the orientation of polymeric crystalline lamella at the surface of thin films can be challenging. Even though atomic force microscopy (AFM) is often sufficient for this analysis, there are cases when imaging is not sufficient to confidently determine lamellar orientation. Here, we used sum frequency generation (SFG) spectroscopy to analyze the lamellar orientation at the surface of semi-crystalline isotactic polystyrene (iPS) thin films.
View Article and Find Full Text PDFMol Pharm
March 2023
Biological Physics Laboratory, School of Physics and Astronomy, University of Manchester, Oxford Road, Schuster Building, Manchester M13 9PL, U.K.
Interfacial adsorption is a molecular process occurring during the production, purification, transport, and storage of antibodies, with a direct impact on their structural stability and subsequent implications on their bioactivities. While the average conformational orientation of an adsorbed protein can be readily determined, its associated structures are more complex to characterize. Neutron reflection has been used in this work to investigate the conformational orientations of the monoclonal antibody COE-3 and its Fab and Fc fragments at the oil/water and air/water interfaces.
View Article and Find Full Text PDFNat Commun
March 2022
CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Peptide hormones and neuropeptides are complex signaling molecules that predominately function through G protein-coupled receptors (GPCRs). Two unanswered questions remaining in the field of peptide-GPCR signaling systems pertain to the basis for the diverse binding modes of peptide ligands and the specificity of G protein coupling. Here, we report the structures of a neuropeptide, galanin, bound to its receptors, GAL1R and GAL2R, in complex with their primary G protein subtypes G and G, respectively.
View Article and Find Full Text PDFACS Appl Mater Interfaces
February 2021
Materials Science and Engineering, School for Engineering of Matter, Transport and Energy, Arizona State University, Tempe, Arizona 85287, United States.
Antibiotic-resistant bacteria are a significant and growing threat to human health. Recently, two-dimensional (2D) nanomaterials have shown antimicrobial activity and have the potential to be used as new approaches to treating antibiotic resistant bacteria. In this Research Article, we exfoliate transition metal dichalcogenide (TMDC) nanosheets using synthetic single-stranded DNA (ssDNA) sequences, and demonstrate the broad-spectrum antibacterial activity of MoSe encapsulated by the T ssDNA sequence in eliminating several multidrug-resistant (MDR) bacteria.
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