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Efficient and low cost detection of harmful volatile organic compounds (VOCs) is a major health and environmental need in industrialized societies. For this, tailor-made porous coordination polymers are emerging as promising molecular sensing materials thanks to their responsivity to a wide variety of external stimuli and could be used to complement conventional sensors. Here, a non-porous crystalline 1D Fe(ii) coordination polymer acting as a porous acetonitrile host is presented. The desorption of interstitial acetonitrile is accompanied by magneto-structural transitions easily detectable in the optical and electronic properties of the material. This structural switch and therefore its (opto)electronic readout are reversible under exposure of the crystal to acetonitrile vapor. This simple and robust iron-based coordination polymer could be ideally suited for the construction of multifunctional sensor devices for volatile acetonitrile and potentially for other organic compounds.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625413 | PMC |
http://dx.doi.org/10.1039/c9sc02522g | DOI Listing |
ACS Appl Mater Interfaces
December 2024
Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.
Silver, as the oldest antibacterial material, has been almost replaced by other alternatives for its insufficient activity or potential side-effects on the ecosystem due to the over-release of Ag ions (Ag). Herein, a facile and general strategy is developed to on-substrate fabricate silver coordination polymer nanowire arrays (Ag CPN) by simply immersing Ag-containing substrates into cationic surfactant solution at room temperature. Such a Ag CPN not only provides high-surface-area nano-biointerfaces for destroying microorganisms via physicomechanical interactions but also acts as a safe Ag reservoir, steadily releasing Ag at a relatively high but safe level (∼40 ppb, but lower than the safe level of 100 ppb).
View Article and Find Full Text PDFChem Sci
December 2024
Department of Chemistry, University of Warwick Coventry CV4 7AL UK
Self-assembling cyclic peptide nanotubes are fascinating supramolecular systems with promising potential for various applications, such as drug delivery, transmembrane ionic channels, and artificial light-harvesting systems. In this study, we present novel pH-responsive nanotubes based on asymmetric cyclic peptide-polymer conjugates. The pH response is introduced by a tertiary amine-based polymer, poly(dimethylamino ethyl methacrylate) (pDMAEMA) or poly(diethylamino ethyl methacrylate) (pDEAEMA) which is protonated at low pH.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Chinese Academy of Sciences, State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350608, P. R. China., CHINA.
Coordination polymers (CPs) are promising for direct X-ray detection and imaging owing to higher designability and outstanding stability, however, it remains a challenge to achieve highly X-ray detection performance, particularly both high sensitivity and low detection limit at the same operating voltage. Herein, we construct a new conjugated CP {[Co(BPTTz)(DIPA)] DMA}n (1, BPTTz = 2,5-bis(pyridine-4-yl)thiazolo[5,4-d]thiazole, H2DIPA = 2,5-diiodoterephthalic acid, DMA = N, N'-dimethylacetamide), with multi-channel charge transfer by regulating the linker mediated electronic-state, which reduces carrier losses resulting from recombination or quenching, enhances the efficiency of charge separation and transfer, thus further optimizes X-ray detection performance. The semiconductor prepared based on this strategy achieves record values including the highest mobility-lifetime product (μτ, 8.
View Article and Find Full Text PDFBiosens Bioelectron
December 2024
School of Medical Science and Technology, Indian Institute of Technology, Kharagpur, 721302, West Bengal, India. Electronic address:
Monitoring HO levels in live cells is essential due to its superior stability and possible severity inside the cell. The quest for a superior platform capable of detecting cellular-level hydrogen peroxide (HO) concentrations without necessitating the use of high-cost enzymes is of utmost importance. Here, the quantification of intracellular HO concentrations has been performed using silver metal polymer-based nonenzymatic electrochemical detection.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Shenzhen institute of advanced technology Chinese Academy of Sciences, Functional Thin Films Research Centre, 1068 Xueyuan Avenue, Shenzhen University Town, 518000, SHENZHEN, CHINA.
Organics electrode materials offer multi-electron reactivity, flexible structures, and redox reversibility, but encounter poor conductivity and durability in electrolytes. To overcome above barriers, we propose a dual elongation strategy of π-conjugated motifs with active sites, involving extended carbazole and electropolymerized crosslinked polymer, which enhances electronic conductivity by the electronic delocalization of electron-withdrawing conjugated groups, boosts theoretical capacity by increasing redox-active site density, and endows robust electrochemical stability attributed to crosslinked organic structures. As a proof-of-concept, 5,11-dihydridoindolo[3,2-b]carbazole (DHIC) is selected as the model cathode material for a dual-ion battery, with elongated carbazole groups functioning both as redox-active centers and polymerization anchors.
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