نتایج جستجو برای: Hexadentate

تعداد نتایج: 157  

2016
Qingchun Zhang Bo Jin Zhaotao Shi Xiaofang Wang Qiangqiang Liu Shan Lei Rufang Peng

A series of novel hexadentate enterobactin analogues, which contain three catechol chelating moieties attached to different molecular scaffolds with flexible alkyl chain lengths, were prepared. The solution thermodynamic stabilities of the complexes with uranyl, ferric(III), and zinc(II) ions were then investigated. The hexadentate ligands demonstrate effective binding ability to uranyl ion, an...

Journal: :Journal of pharmaceutical sciences 2000
R A Yokel A M Fredenburg P W Durbin J Xu M K Rayens K N Raymond

Bidentate hydroxypyridinone chelators effectively complex and facilitate excretion of trivalent iron. To test the hypothesis that hexadentate chelators are more effective than bidentate chelators at low concentrations, urinary and biliary Fe excretions were determined in Fe-loaded rats before and after administration of a bidentate chelator, Pr-(Me-3,2-HOPO), or its hexadentate analogue, TREN-(...

Journal: :Dalton transactions 2015
Peter Comba Henning Rudolf Hubert Wadepohl

Reported is the new bispidine-derived hexadentate ligand (L = 3-(2-methylpyridyl)-7-(bis-2-methylpyridyl)-3,7-diazabicyclo[3.3.1]nonane) with two tertiary amine and four pyridine donor groups. This ligand can form heterodinuclear and mononuclear complexes and, in the mononuclear compounds discussed here, the ligand may coordinate as a pentadentate ligand, with one of the bispyridinemethane-base...

Journal: :Inorganic chemistry 2011
Chang-Jin Qin Lloyd James Jy D Chartres Leighton J Alcock Kimberley J Davis Anthony C Willis Alan M Sargeson Paul V Bernhardt Stephen F Ralph

The bicyclic hexaamine "cage" ligand Me(8)tricosaneN(6) (1,5,5,9,13,13,20,20-octamethyl-3,7,11,15,18,22-hexaazabicyclo[7.7.7]tricosane) is capable of encapsulating octahedral metal ions, yet its expanded cavity allows the complexed metal to adopt a variety of geometries comprising either hexadentate or pentadentate coordination of the ligand. When complexed to Cu(II) the lability of the metal r...

Journal: :Dalton Transactions 2023

In this paper we use mono- and bi-metallic complexes, based on earth-abundant, cheap benign zinc, for the synthesis of sustainable aliphatic semi-aromatic polyesters. Tridentate hexadentate aldimine-thioetherphenolate ligands...

Journal: :Chemical communications 2015
Maria Moula Karimdjy Gaylord Tallec Pascal H Fries Daniel Imbert Marinella Mazzanti

The water soluble tris-aqua complex [Gd(dhqN-SO3)(H2O)3](3-) based on a hexadentate hydroxyquinoline ligand shows high thermodynamic stability and high relaxivity (12.54 mM(-1) s(-1) at 1.2 T). Its non-covalent confinement in 25 nm silica nanoparticles prevents transmetallation and endogenous anion binding and leads to higher relaxivity over a wide range of magnetic fields.

Journal: :Dalton transactions 2007
Steven Kealey Nicholas J Long Andrew J P White Antony D Gee

A new tetrakis(pyrazolyl)borate ligand bearing triphenylphosphine oxide moieties appended to the 3-position of the pyrazolyl rings is reported and shown to display varied coordination chemistry from tridentate N(2)O coordination with thallium to hexadentate N(3)O(3) coordination with europium.

2010
Pierre-Marc Léo Christophe Morin Christian Philouze

Conversion of a myo-inositol derivative into a scyllo-inositol-derived scaffold with C₃(v) symmetry bearing three axial pyridyl appendages is presented. This pre-organized hexadentate ligand allows complexation of silver(I). The crystal structure of the complex was established.

Journal: :European Journal of Inorganic Chemistry 2021

Journal: :Inorganic chemistry 2006
Miquel Costas Xavi Ribas Albert Poater Josep Maria López Valbuena Raül Xifra Anna Company Miquel Duran Miquel Solà Antoni Llobet Montserrat Corbella Miguel Angel Usón José Mahía Xavier Solans Xiaopeng Shan Jordi Benet-Buchholz

Density functional theory (DFT) calculations have been carried out for a series of Cu(I) complexes bearing N-hexadentate macrocyclic dinucleating ligands and for their corresponding peroxo species (1c-8c) generated by their interaction with molecular O2. For complexes 1c-7c, it has been found that the side-on peroxodicopper(II) is the favored structure with regard to the bis(mu-oxo)dicopper(III...

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