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Poly ligands

Polyphenylene polymers can be prepared by this coupling. For example, the preparation of poly(/i-quaterphenylene-2,2 -dicarboxylic acid) (643) was carried out using aqueous NaHCO and a water-soluble phosphine ligand (DPMSPP)[5I I]. Branched polyphenylene was also prepared[5l2). [Pg.219]

Pyrazoles, and some indazoles, substituted on the nitrogen by B, Al, Ga, In, Si, Ge, Sn, P and Hg are known. Poly(pyrazol-1 -yl)borates have been studied by Trofimenko (72CRV497) who found that they were excellent ligands (Section 4.04.2.1.3(vi)). The parent ligands (282), (283) and (284) are available by the reaction of an alkali metal borohydride with pyrazole, the extent of substitution depending on the reaction temperature (Scheme 22). [Pg.235]

Poly(phenylenepyrazoles), 5, 300 Polypyrazoles, 5, 300 N-substituted, 5, 300 Polypyrazolines, 5, 300 Poly(pyrazol-l-yl) borates as ligands, 5, 225, 235 Polypyrroles applications, 4, 376 Polypyrrole tetrafluoroborate conductors, 1, 355 Polysaccharides as pharmaceuticals, 1, 152 Poly-2,5-selenienylenes applications, 4, 971 Polysilacyclopentanes, 1, 609 Polysufides macrocyclic... [Pg.748]

Recent advances in complexes of group VIB metals (Mo, W) with poly-(pyrazolyl)borate ligands 98MI2. [Pg.252]

Self-assembly of poly iodide networks on templates with crown ethers, thia- and thiazacrown ethers as ligands 98CSR195. [Pg.269]

Polymalatase may be useful for the tayloring of /3-poly(malic acid) and its derivatives, and for analytical purposes. If the hydrolase is arrested at points of polymer branches or covalently/physically attached ligands, the hydrolase can be used in studies analogous to those known for DNA and exonucleases. [Pg.102]

Poly (macrocyclic) compounds. The analytical application of compounds such as crown polyethers and cryptands is based on their ability to function as ligands and form stable stoichiometric complexes with certain cations. Special importance is due to their preference for alkali metal ions which do not form complexes with many other ligands. A number of these compounds are commercially available and their properties and analytical applications have been described by Cheng et a/.11... [Pg.172]

These carbonyl chloride-activated carriers are unstable on storage, so ligand coupling to them has to be undertaken immediately after chemisorption of the copolymer. To overcome this drawback, more stable activated carriers have been synthesized by treating aminopropyl-silicas with poly(p-nitrophenyl acrylate) and acetic anhydride. [Pg.155]

Poly (p-nitrophenyl acrylate)-coated wide-pore glass (WPG) was also used as an activated carrier for the immobilization of biospecific ligands and enzymes, A detailed description of properties of these sorbents and catalysts as well as some specific features of their functioning is given in Sect. 6. [Pg.158]

Porous glass (PG) modified with covalently adsorbed poly(p-nitrophenyl acrylate), as described in Sect. 4.1, turned out to be a highly suitable carrier for immobilization of various biospecific ligands and enzymes. When the residual active ester groups of the carrier were blocked by ethanolamine, the immobilized ligands when bound to the solid support via hydrophilic and flexible poly(2-hydroxyethyl acrylamide). The effective biospecific binding provided by the ligands... [Pg.170]

A great variety of suitable polymers is accessible by polymerization of vinylic monomers, or by reaction of alcohols or amines with functionalized polymers such as chloromethylat polystyrene or methacryloylchloride. The functionality in the polymer may also a ligand which can bind transition metal complexes. Examples are poly-4-vinylpyridine and triphenylphosphine modified polymers. In all cases of reactively functionalized polymers, the loading with redox active species may also occur after film formation on the electrode surface but it was recognized that such a procedure may lead to inhomogeneous distribution of redox centers in the film... [Pg.53]

Stmcturally novel pyrazole derivatives include the propellene 2,3,4,5,6-pentakis(pyrazol-r-yl)pyridine 1 and the corresponding 3 ,5 -dimethylpyrazole derivative 2<96T11075>. Poly(pyrazol-l-ylmethyl)benzenes, such as 3, have been prepared as multidentate ligands <95AJC1587>. Solid phase synthesis of structurally diverse 1-phenylpyrazolones was reported, with application to combinatorial synthesis <96SL667>. [Pg.148]

This review deals with the chemistry and coordination complexes of isoelectronic analogues of common oxo-anions of phosphorus such as PO3, POl", RPOl" and R2POy. The article begins with a discussion of homoleptic systems in which all of the 0x0 ligands are replaced by imido (NR) groups. This is followed by an account of heteroleptic phosphorus-centered anions, including [RN(E)P(/<-NR )2P(E)NR]2-, [EP(NR)3]3-, [RP(E)(NR)2] and [R2P(E)(NR )] (E=0,S, Se, Te). The emphasis is on the wide variety of coordination modes exhibited by these poly-dentate ligands, which have both hard (NR) and soft (S, Se or Te) centers. Possible applications of their metal complexes include new catalytic systems, coordination polymers with unique properties, and novel porous materials. [Pg.143]

Diamine 108 led to 95% ee for the alkylation of l,3-diphenyl-2-propenyl acetate with 90% yield. By polycondensation with a diacid chloride or polyaddition with a diisocyanate, this ligand led, respectively, to an insoluble poly(amide) 109 or poly(urea) 110 with excellent yields. Poly(amide) 109 gave a better ee (80%) than poly(urea) 110 (38%), albeit with a lower conversion (respectively, 38 and 72%), when they were used as palladium hgands... [Pg.140]

Chiral lactones were also formed by cyclocarbonylation [ 122] with chiral catalysts, such as Pd-poly-L-leucine catalytic system. For example, but-2-en-l-ol led to the corresponding cychc chiral lactone in the presence of Pd catalysts with chiral ligands (Scheme 33). About 10 mol% of Pd(II) chloride... [Pg.252]


See other pages where Poly ligands is mentioned: [Pg.177]    [Pg.483]    [Pg.156]    [Pg.157]    [Pg.111]    [Pg.177]    [Pg.483]    [Pg.156]    [Pg.157]    [Pg.111]    [Pg.207]    [Pg.316]    [Pg.163]    [Pg.225]    [Pg.310]    [Pg.1005]    [Pg.1056]    [Pg.159]    [Pg.99]    [Pg.123]    [Pg.152]    [Pg.185]    [Pg.17]    [Pg.137]    [Pg.156]    [Pg.202]    [Pg.208]    [Pg.223]    [Pg.244]    [Pg.253]    [Pg.587]    [Pg.260]    [Pg.186]    [Pg.131]    [Pg.18]    [Pg.69]    [Pg.321]    [Pg.59]   
See also in sourсe #XX -- [ Pg.9 ]




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Chiral poly-NHC ligands

Nickel, poly ligands

Poly , BINOL ligands

Poly borate ligand

Poly dentate Nitrogen Donor Ligands

Poly methane ligands

Poly(l-pyrazolyl)alkane Ligands

Poly(phosphine) Multidentate Ligands

Poly-NHCs ligands

Poly-NHCs ligands chiral

Poly-NHCs ligands pincer

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