Results 11 to 20 of about 13,279 (251)

2,3-Dibutoxynaphthalene-based tetralactam macrocycles for recognizing precious metal chloride complexes

open access: yesBeilstein Journal of Organic Chemistry, 2019
Two new tetralactam macrocycles with 2,3-dibutoxynaphthalene groups as sidewalls have been synthesized and characterized. The macrocycle containing isophthalamide bridges can bind square-planar chloride coordination complexes of gold(III), platinum(II ...
Li-Li Wang   +3 more
doaj   +1 more source

Structure–Property Relationship of Macrocycles in Organic Photoelectric Devices: A Comprehensive Review

open access: yesNanomaterials, 2023
Macrocycles have attracted significant attention from academia due to their various applications in organic field-effect transistors, organic light-emitting diodes, organic photovoltaics, and dye-sensitized solar cells.
Chunxiao Zhong   +9 more
doaj   +1 more source

Photosensitizers Mediated Photodynamic Inactivation against Fungi

open access: yesNanomaterials, 2021
Superficial and systemic fungal infections are essential problems for the modern health care system. One of the challenges is the growing resistance of fungi to classic antifungals and the constantly increasing cost of therapy.
Daniel Ziental   +4 more
doaj   +1 more source

Crystal structure of cyclo-tris(μ-3,4,5,6-tetrafluoro-o-phenylene-κ2C1:C2)trimercury–tetracyanoethylene (1/1)

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
The title compound, [Hg3(C6F4)3]·C6N4, contains one molecule of tetracyanoethylene B per one molecule of mercury macrocycle A, i.e., A•B, and crystallizes in the monoclinic space group C2/c.
Raúl Castañeda   +2 more
doaj   +1 more source

Symmetric Macrocycles by a Prins Dimerization and Macrocyclization Strategy [PDF]

open access: yesOrganic Letters, 2009
A tandem dimerization/macrocyclization reaction utilizing the Prins cyclization has been developed. This reaction develops molecular complexity through the formation of highly substituted dimeric tetrahydropyran macrocycles. Mild conditions utilizing rhenium(VII) catalysts were explored for aromatic substrates, while harsher Lewis acidic conditions ...
Michael R, Gesinski   +2 more
openaire   +2 more sources

A ferrocene redox-active triazolium macrocycle that binds and senses chloride

open access: yesBeilstein Journal of Organic Chemistry, 2012
A ferrocene bis(triazole) macrocycle was synthesised in good yield by the Eglinton coupling of an acyclic bis(alkyne) precursor and characterised in the solid state by X-ray crystallography. Alkylation gives the corresponding triazolium macrocycle, which
Nicholas G. White, Paul D. Beer
doaj   +1 more source

Computational Site Saturation Mutagenesis of Canonical and Non-Canonical Amino Acids to Probe Protein-Peptide Interactions

open access: yesFrontiers in Molecular Biosciences, 2022
Technologies for discovering peptides as potential therapeutics have rapidly advanced in recent years with significant interest from both academic and pharmaceutical labs.
Jeffrey K. Holden   +4 more
doaj   +1 more source

Spectral manifestation of substitution of out-of-plane ligands in metallophtalocyanines

open access: yesEPJ Web of Conferences, 2017
In our study, we demonstrate the splitting effect of long-wavelength bands in absorption spectra (excitation of fluorescence) of the series of Zn(II), Ti(IV), Zr(IV) and Hf(IV) phthalocyanines at low temperatures.
Starukhin A.   +6 more
doaj   +1 more source

Size-Induced Highly Selective Synthesis of Organometallic Rectangular Macrocycles and Heterometallic Cage Based on Half-Sandwich Rhodium Building Block

open access: yesMolecules, 2022
The controlled synthesis of organometallic supramolecular macrocycles cages remains interesting and challenging work in the field of supramolecular chemistry.
Li-Long Dang   +6 more
doaj   +1 more source

Formation of a macrocycle from dichlorodimethylsilane and a pyridoxalimine Schiff base ligand

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2021
The reaction of dichlorodimethylsilane with a polydentate Schiff base ligand derived from pyridoxal and 2-ethanolamine yielded the macrocyclic silicon compound (8E,22E)-4,4,12,18,18,26-hexamethyl-3,5,17,19-tetraoxa-8,13,22,27-tetraaza-4,18-disilatricyclo[
Uwe Böhme   +2 more
doaj   +1 more source

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