Results 201 to 210 of about 210,013 (270)
Alkali metal cation effects for rapid C-H activation by iron(0) complexes. [PDF]
Hidalgo N +6 more
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Host-Guest Chemistry as a Supramolecular Engine for Iontronic Transduction in Nanochannels. [PDF]
Hernández Parra LM +7 more
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Adaptive Zinc-Amide Catalysis Enables C(sp<sup>2</sup>)-O Cross-Coupling of Aryl Fluorides with Alcohols. [PDF]
Manna S, Kavil NS, Rit A.
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Advances in Materials for Strontium-Yttrium Separation: A Comprehensive Review. [PDF]
Xu M +6 more
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Crown ethers in hydrogenated graphene
Physical Chemistry Chemical Physics, 2021Graphane could serve as an ideal platform to rigidify the highly flexible crown ethers, which will greatly improve the binding strength and selectivity of crown ethers with metal cations and open up new applications for crown ethers and graphane.
Kai Guo +8 more
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Crown Ethers: Novel Permeability Enhancers for Ocular Drug Delivery? [PDF]
Crown ethers are cyclic molecules consisting of a ring containing several ether groups. The most common and important members of this series are 12-crown-4 (12C4), 15-crown-5 (15C5), and 18-crown-6 (18C6).
Rouslan Moustafine +2 more
exaly +2 more sources
UNSATURATED CROWN ETHERS: STILBENO-CROWN ETHERS
Chemistry Letters, 1982Abstract Stilbenocrown ethers 3a,c and 4a,b were synthesized in a cyclization reaction of benzoin with oligoethylene glycol ditosylates(2a-c) under a phase-transfer condition. Extractions of aqueous alkali picrates(Na+–Cs+) were examined with the distilbenocrown ethers 4a,b, the partially-hydrogenated tetraphenylcrown ethers 6a,b and the
Yoshihisa Inoue +4 more
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From Crown Ethers to Zeolites: Reaction of EtAlCl2 with Crown Ethers
Journal of Inclusion Phenomena, 1984In contrast to aluminum alkyls, alkyl aluminum halides such as EtAlCl2 react with crown ethers to form cation-anion pairs which exhibit the liquid clathrate effect. Specifically, [12-C-4-·AlCl2][AlCl3Et] and [18-C-6·AlCl2][AlCl3Et] have been isolated and characterized by X-ray diffraction techniques.
Jerry L. Atwood +5 more
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Tetrahedron, 1980
Abstract The stability constants for the 1:1 complexes of 1,7,10,16-tetraoxa-4, 13-diazacyclooctadecane and 4,7,13,16,21,24-hexaoxa-1, 10-diazabicyclo[8,8,8]hexacosane with Na+, K+, Rb+ and Cs+ have been determined in acetonitrile at 25.0°C by conductivity measurements. The stability constants are considerably higher, and the selectivity is different,
S. Kulstad, L.Å. Malmsten
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Abstract The stability constants for the 1:1 complexes of 1,7,10,16-tetraoxa-4, 13-diazacyclooctadecane and 4,7,13,16,21,24-hexaoxa-1, 10-diazabicyclo[8,8,8]hexacosane with Na+, K+, Rb+ and Cs+ have been determined in acetonitrile at 25.0°C by conductivity measurements. The stability constants are considerably higher, and the selectivity is different,
S. Kulstad, L.Å. Malmsten
openaire +1 more source

