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A series of diphosphine Re(I) complexes - have been designed via decoration of the archetypal core {Re(CO)(N^N)} through the installations of the phosphines and bearing the terminal double bond, where N^N = 2,2'-bipyridine (), 4,4'-di-tert-butyl-2,2'-bipyridine () or 2,9-dimethyl-1,10-phenanthroline () and = diphenylvinylphosphine, and = 4-(diphenylphosphino)styrene. These complexes were copolymerized with the corresponding N-vinylpyrrolidone-based Macro-RAFT agents of different polymer chain lengths to give water-soluble copolymers of low-molecular ) and high-molecular block-copolymers containing rhenium complexes. Compounds -, as well as the copolymers and , demonstrate phosphorescence from a MLCT excited state typical for this type of chromophores. The copolymers and display weak sensitivity to molecular oxygen in aqueous and buffered media, which becomes almost negligible in the model physiological media. In cell experiments with CHO-K1 cell line, and displayed significantly reduced toxicity compared to the initial complex and internalized into cells presumably by endocytic pathways, being eventually accumulated in endosomes. The sensitivity of the copolymers to oxygen examined in CHO-K1 cells via phosphorescence lifetime imaging microscopy (PLIM) proved to be inessential.
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http://dx.doi.org/10.3390/molecules28010348 | DOI Listing |
Langmuir
September 2025
Federal University of São Paulo, Laboratory of Hybrid Materials, Diadema, São Paulo 09913-030, Brazil.
This study demonstrates the successful fabrication of nanostructured Langmuir-Blodgett (LB) films combining the conjugated copolymer poly(9,9-dioctylfluorene--3,4-ethylenedioxythiophene) (PDOF--PEDOT) with spherical and triangular silver nanoparticles (AgNP). The LB technique allowed precise control over the molecular arrangement and distribution of the nanoparticles at the air-water interface, resulting in compact, reproducible and structurally ordered nanocomposite films. The structural and morphological properties of the interfacial monolayers and LB films were investigated using surface pressure-area isotherms, Brewster angle microscopy, polarization modulation infrared reflection-absorption spectroscopy (PM-IRRAS) and quartz crystal microbalance.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Materials Science and Engineering, Iowa State University, Ames, Iowa 50011, United States.
Distinctive polymer brushes (PBs) play a crucial role in providing a nonpreferential (neutral) surface for vertical orientation of block copolymers (BCPs). This bottom-up approach effectively aligns the formation of vertical lamellar and cylinder lattice structures from the BCP, which is crucial for nanopatterning and other applications. In conventional BCP self-assembly techniques, random copolymer brushes are commonly employed to achieve substrate neutrality.
View Article and Find Full Text PDFACS Macro Lett
September 2025
State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Fudan University, Shanghai 200433, China.
Poly(3-hexylthiophene) (P3HT)-based complex topological copolymers have attracted a great deal of attention for their unique electrical and optical properties. In this contribution, the P3HT-based Janus fibers with controlled lengths were innovatively prepared by sequential crystallization-driven self-assembly (CDSA) of poly(--butylstyrene)--polyisoprene--poly(3-hexylthiophene) (PBS--PI--P3HT) triblock copolymer, cross-linking of the interlayer PI region, and dissociation of fibers in good solvent. The comprehensive characterizations showed that the PBS/P3HT Janus fibers have nearly half the width of PBS--PI--P3HT fibers and fiber lengths close to or slightly shorter than those of PBS--PI--P3HT fibers, indicating that the Janus fibers with adjustable lengths could be prepared in a large window range.
View Article and Find Full Text PDFJ Mater Chem B
September 2025
School of Materials Science and Engineering, Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates, South China University of Technology, Guangzhou, 510640, China.
Antibacterial photodynamic therapy offers a promising approach for combating both susceptible and multidrug-resistant pathogens. However, conventional photosensitizers have limitations in terms of poor binding specificity and weak penetration for pathogens. In this study, we developed synergistic photobactericidal polymers that integrate hydrophilic toluidine blue O (TBO) with the lipophilic penetration enhancer citronellol (CT).
View Article and Find Full Text PDFChemistry
September 2025
Beijing National Laboratory for Molecular Sciences, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Center for Soft Matter Science and Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, China.
Sequence-controlled polyester-based alternating copolymers have attracted significant interest due to their biocompatibility, biodegradability, closed-loop recyclability, and hydrolytic degradability, offering broad potential in biomedical and sustainable materials. Among the available strategies, regioselective ring-opening polymerization (ROP) of asymmetric cyclic di(thio)esters and cyclic(ester-amide)s has emerged as a promising approach for constructing alternating copolymers with precise sequence- and stereo-control, structural diversity, and tunable properties. This review classifies asymmetric cyclic monomers into two categories: (1) monomers with two aliphatic ester bonds, where regioselectivity is mainly dictated by steric differences and typically requires tailored metal catalysts; and (2) monomers with chemically distinct reactive sites (e.
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