The long diphosphine 5,11-diphenylphosphanyl-25,26-dipropyloxy-27,28-bis(2-propenyloxy) calix[4]arene (cone) (5), in which the two phosphorus atoms are separated by a semi-rigid linking unit, was prepared in four steps starting from calix[4]arene. Reaction of 5 with AuCl(SEt(2)) or [RuCl(2)(p-cymene)](2) led to calixarenes bearing two metallated pendant arms, [5·(AuCl)(2)] and [5·{RuCl(2)(p-cymene)}(2)], respectively. In the presence of AgBF(4) or [Ni(C(5)H(5))(1,5-cyclooctadiene)]BF(4), diphosphine 5 displayed a marked tendency to form oligomeric material, but under high dilution conditions dimeric species were obtained selectively. The inability of 5 to form chelate complexes was further illustrated by its reaction with [PdCl(2)(1,5-cyclooctadiene)(2)], which led quantitatively to a rare complex in which a diphosphine spans across the dinuclear [PdCl(μ-Cl)(2)PdCl] unit.
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Inorg Chem
January 2021
Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
The first boron complexes of porphycenes, structural isomers of porphyrin, are reported. They are synthesized in good yields by reacting the free-base porphycene ligands with BF·EtO through a microwave-assisted method. Depending on the substituent group of porphycenes, two different coordination structures, mono- and diboron porphycenes, are obtained simultaneously.
View Article and Find Full Text PDFChem Sci
February 2020
Department of Chemistry , University of California, Berkeley , Berkeley , CA 94720-1460 , USA . Email:
A dicopper complex featuring a symmetrically bridging nitrile ligand and supported by a binucleating naphthyridine-based ligand, [Cu( : -MeCN)DPFN](NTf), was treated with phosphaalkynes (RC[triple bond, length as m-dash]P, isoelectronic analogues of nitriles) to yield dicopper complexes that exhibit phosphaalkynes in rare : binding coordination modes. X-ray crystallography revealed that these unusual "tilted" structures exist in two isomeric forms (R "up" R "sideways"), depending on the steric profile of the phosphaalkyne's alkyl group (R = Me, Ad, or Bu). Only one isomer is observed in both solution and the solid state for R = Me (sideways) and Bu (up).
View Article and Find Full Text PDFRSC Adv
December 2019
ICMol, Departamento de Química Inorgánica, Universidad de Valencia C/Catedrático José Beltrán 2 46980 Paterna Spain
Two binucleating hezaaza macrocycles containing a pyridinol spacer have been prepared and characterised. Protonation studies indicate the deprotonation of the phenol group at relatively low pH values with the concomitant occurrence of a keto-enolic equilibrium. These ligands readily form binuclear Cu and Zn complexes as denoted by potentiometric and spectroscopic studies.
View Article and Find Full Text PDFInorg Chem
June 2015
†Department of Chemistry, Indian Institute of Technology, Kharagpur 721 302, India.
A [Ni(II)4] staircase complex was serendipitously prepared from the reaction of the binucleating Schiff base proligand 2,6-bis[[(3-hydroxypropyl)imino]methyl]-4-methylphenol (H3L2) and 3,5-dimethylpyrazole (Me2pzH) with nickel(II) nitrate in a reaction at room temperature, initially aimed to yield a dinuclear complex. From a room temperature metal ion/ligand reaction, the proligand H3L2 in situ transformed to modified forms HL3(2-) and HL4(2-), allowing the [Ni4] formation. Variable-temperature magnetic behavior of a [Ni4] complex reveals antiferromagnetic interactions with stabilization of a diamagnetic ground state (ST = 0).
View Article and Find Full Text PDFJ Am Chem Soc
March 2014
Department of Chemistry, University of California, Berkeley, California 94720, United States.
A series of actinide-transition metal heterobimetallics has been prepared, featuring thorium, uranium, and cobalt. Complexes incorporating the binucleating ligand N[ο-(NHCH2P(i)Pr2)C6H4]3 with either Th(IV) (4) or U(IV) (5) and a carbonyl bridged [Co(CO)4](-) unit were synthesized from the corresponding actinide chlorides (Th: 2; U: 3) and Na[Co(CO)4]. Irradiation of the resulting isocarbonyls with ultraviolet light resulted in the formation of new species containing actinide-metal bonds in good yields (Th: 6; U: 7); this photolysis method provides a new approach to a relatively unusual class of complexes.
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