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Studies of Halogen Bonding Induced by Pentafluorosulfanyl Aryl Iodides: A Potential Group of Halogen Bond Donors in a Rational Drug Design [PDF]

open access: yesMolecules, 2019
The activation of halogen bonding by the substitution of the pentafluoro-λ6-sulfanyl (SF5) group was studied using a series of SF5-substituted iodobenzenes.
Yuji Sumii   +3 more
doaj   +2 more sources

Research on Synthesis, Structure, and Catalytic Performance of Tetranuclear Copper(I) Clusters Supported by 2-Mercaptobenz-zole-Type Ligands [PDF]

open access: yesMolecules
Tetrahedral copper(I) clusters [Cu4(MBIZ)4(PPh3)2] (2), [Cu4(MBOZ)4(PPh3)4] (6) (MBIZ = 2-mercaptobenzimidazole, MBOZ = 2-mercaptobenzoxazole) were prepared by regulation of the copper-thiolate clusters [Cu6(MBIZ)6] (1) and [Cu8(MBOZ)8I]− (5) with PPh3 ...
Tingyu Zhu   +3 more
doaj   +2 more sources

Structural Features of Dihenzoyldioxy-Iodobenzenes

open access: yesCHIMIA, 1972
Covalent (I) rather than ionic (II) structure has been assigned to dihenzoyldioxy-iodobenzenes.
Božo Plesničar
doaj   +2 more sources

Tautomeric Equilibrium of an Asymmetric β-Diketone in Halogen-Bonded Cocrystals with Perfluorinated Iodobenzenes

open access: yesCrystals, 2021
In order to study the effect of halogen bond on tautomerism in β-diketones in the solid-state, we have prepared a series of cocrystals derived from an asymmetric β-diketone, benzoyl-4-pyridoylmethane (b4pm), as halogen bond acceptor and perfluorinated ...
Valentina Martinez   +3 more
doaj   +1 more source

The Amine Group as Halogen Bond Acceptor in Cocrystals of Aromatic Diamines and Perfluorinated Iodobenzenes

open access: yesCrystals, 2021
In order to study the proclivity of primary amine groups to act as halogen bond acceptors, three aromatic diamines (p-phenylenediamine (pphda), benzidine (bnzd) and o-tolidine (otol)) were cocrystallised with three perfluorinated iodobenzenes (1,4 ...
Erik Uran   +4 more
doaj   +1 more source

Pyridine-promoted dediazoniation of aryldiazonium tetrafluoroborates: Application to the synthesis of SF5-substituted phenylboronic esters and iodobenzenes

open access: yesBeilstein Journal of Organic Chemistry, 2015
Pyridine promotes dediazoniation of aryldiazonium tetrafluoroborates. The formed aryl radicals were trapped with B2pin2, iodine, or tetrahydrofuran to afford boronic esters, iodobenzenes and benzenes, respectively.
George Iakobson   +3 more
doaj   +1 more source

Polymer-supported Pd(0) catalyst for copper- and ligand-free Sonogashira reactions in aqueous media

open access: yesGreen Processing and Synthesis, 2012
The treatment of commercially available polymethyl methacrylate (PMMA) microspheres with palladium (Pd)Cl2 and formaldehyde, generated supported Pd(0)-PMMA with 0.79 (wt)% catalyst loading.
Yi Wen-Bin   +3 more
doaj   +1 more source

One-Pot Synthesis of Hypervalent Diaryl(iodo)bismuthanes from o-Carbonyl Iodoarenes by Zincation

open access: yesHeteroatom Chemistry, 2019
Diaryl(iodo)bismuthanes possessing a hypervalent C=O•••Bi–I bond were conveniently synthesized in a one-pot reaction by using arylzinc reagents generated from o-carbonyl iodobenzenes and zinc powder under ultrasonication.
Toshihiro Murafuji   +6 more
doaj   +1 more source

Photopolymerization of Methyl Methacrylate Initiated by Iodobenzene– Triethylamine and Iodobenzene–Sodium Thiosulfate Systems [PDF]

open access: yesPolymer Journal, 1972
The photopolymerization of methyl methacrylate was investigated in both iodobenzene–triethylamine and iodobenzene–Sodium thiosulfate systems. The polymerization reactions proceeded according to a radical mechanism, and were initiated by the phenyl radical which was generated by photolysis of iodobenzene.
Sumihiro Sakai   +2 more
openaire   +1 more source

3,5-Bis(trifluoromethyl)iodobenzene [PDF]

open access: yes, 2009
InChI = 1S/C8H3F6I/c9-7(10,11)4-1-5(8(12,13)14)3-6(15)2-4/h1-3H InChIKey = VDPIZIZDKPFXLI-UHFFFAOYSA-N (reagent used as a versatile allylation or arylation component) Physical Data: bp 59–61 °C (10 mmHg); fp 74 °C; d 1.919 g cm^(−3). Solubility: sol DMF, acetonitrile, toluene, and most organic solvents.
Chang, Shuh-Kuen, Oh, Young In
openaire   +2 more sources

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