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Two novel luminescent hetero-trinuclear complexes [Pt2Ag(μ-dpppy)2(C≡CC6H4R-4)4](ClO4) (R = H, 1; R = CH3, 2; dpppy = 2,6-bis(diphenylphosphino)pyridine) were synthesized by the self-assembly reaction between [Pt(C[triple bond, length as m-dash]CC6H4R-4)4](2-) and [Ag2(μ-dpppy)3](2+) and characterized by elemental analyses, electrospray ionization mass spectrometry, and (1)H NMR and (31)P{(1)H} NMR spectroscopy and by X-ray crystallography for complex 2. Two Pt2Ag complexes show strong luminescence in the solid state, but exhibit weak emission in CH2Cl2 solution and in acetonitrile-water (1 : 1, v : v) solution at room temperature. To overcome the limitations of low water solubility and weak emission in solutions, a new kind of luminescent Pt2Ag@SiO2 nanoparticles was prepared by incorporating the new Pt2Ag acetylides into monodisperse silica nanoparticles. It is noted that Pt2Ag@SiO2 nanoparticles exhibit strong luminescence in aqueous solution, and cyanide anions tend to decrease their luminescence intensity in NaHCO3-NaOH buffer solution. Based on this, a novel nanosensor for highly sensitive detection of cyanide anions was developed in the range of 0.1-10.0 μM.
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http://dx.doi.org/10.1039/c4dt00552j | DOI Listing |
J Pharmacol Sci
January 2025
Department of Pathological and Molecular Pharmacology, Faculty of Pharmacy, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, 569-1094, Japan.
Nitric oxide (NO)-donor drugs, which stimulate reduced form of soluble guanylate cyclase (sGC), have different efficacy to the arteries and veins. This study examined whether sGC activators, which activate oxidized/apo sGC, also have arteriovenous selectivity similar to that of NO-donor drugs. The mechanical responses of the isolated blood vessels were assessed using the organ chamber technique and protein expression was verified using western blotting.
View Article and Find Full Text PDFJ Nat Prod
December 2024
Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093-0358, United States.
Marine sponge diterpenoid isonitriles are exceptional nitrogenous natural products that exhibit antiplasmodial activity. Their biosynthesis presents a biosynthetic puzzle: how do the elements of NC engage terpenyl carbocations in isoprenoid secondary metabolism, and what is the biosynthetic precursor of the NC group? Cyanoformic acid (NC-COOH, ) is proposed as a plausible delivery vehicle of NC that resolves a paradox in the commonly held proposition that an inorganic cyanide anion, CN, terminates terpenoid isonitrile (TI) biosynthesis. DFT calculations of NC-COOH and its conjugate base, cyanoformate, NC-COO (), support high nucleophilicity at N and explain bond-forming constitutionality: attack at N and formation of an isonitrile over its nitrile isomer.
View Article and Find Full Text PDFInt J Mol Sci
November 2024
Departamento de Química y Biología, División de Ciencias Básicas, Universidad del Norte, Km 5 vía Puerto Colombia, Barranquilla 081007, Colombia.
This work describes the synthesis and characterization of new quinolone-benzothiazole hybrids, the study of their aggregation-induced emission (AIE) properties, and the use of these systems as efficient fluorescent probes for cyanide ions. These conjugated derivatives are linked through a double bond favoring electronic communication, and together with their planar geometry, can strongly aggregate under solvophobic environments, leading to aggregation and exhibiting significant AIE behavior. The double bond between electroactive units is prone to nucleophilic addition reactions by cyanide ions, selectively, conducive to turning off the fluorescence properties, making this hybrid system an efficient probe for cyanide ions.
View Article and Find Full Text PDFJ Org Chem
December 2024
Department of Chemistry, Indian Institute of Engineering Science and Technology, Shibpur, Botanic Garden, Howrah 711103, India.
Herein, we describe a Zn-catalyzed atom-economical, inexpensive, and sustainable method for preparing a broad spectrum of substituted olefins utilizing alcohols as the main precursor. Using a Zn(II) complex [ZnLCl] () of the redox-noninnocent ligand 2-((4-chlorophenyl)diazenyl)-1,10-phenanthroline (), various ()-olefins were prepared in good yields by coupling alcohols with sulfones and aryl cyanides under an inert atmosphere. Under an aerial atmosphere, vinyl nitriles were isolated in up to 82% yield reacting alcohols with benzyl cyanides in the presence of .
View Article and Find Full Text PDFPhotochem Photobiol Sci
December 2024
Ivanovo State University of Chemistry and Technology, Sheremetevskii Pr. 7, Ivanovo, 153000, Russia.
Colorimetric chemosensors L and L, based on isoniazid hydrazones, have been designed for the highly sensitive and selective recognition of CN ion. Competing experiments were conducted with various other anions such as F, Cl, Br, I, SCN, ClO, ClO, NO, HPO, SO, and HSO in an acetonitrile solution. In the UV-Vis spectra, a bathochromic shift in the absorption bands of both hydrazones was observed following the addition of cyanide.
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