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Amidines chelating ligands

Chromium, (ri6-benzene)tricarbonyl-stereochemistry nomenclature, 1,131 Chromium complexes, 3,699-948 acetylacetone complex formation, 2,386 exchange reactions, 2,380 amidines, 2,276 bridging ligands, 2,198 chelating ligands, 2,203 anionic oxo halides, 3,944 applications, 6,1014 azo dyes, 6,41 biological effects, 3,947 carbamic acid, 2,450 paddlewheel structure, 2, 451 carboxylic acids, 2,438 trinuclear, 2, 441 carcinogenicity, 3, 947 corroles, 2, 874 crystal structures, 3, 702 cyanides, 3, 703 1,4-diaza-1,3-butadiene, 2,209 1,3-diketones... [Pg.102]

Homoleptic lanthanide(III) tris(amidinates) and guanidinates are among the longest known lanthanide complexes containing these chelating ligands. In this area the carbodiimide insertion route is usually not applicable, as simple, well-defined lanthanide tris(alkyls) and tris(dialkylamides) are not readily available. A notable exception is the formation of homoleptic lanthanide guanidinates from... [Pg.234]

Chromium complexes acetylacetone complex formation, 386 exchange reactions, 380 amidines, 276 bridging ligands, 198 chelating ligands, 203 carbamic add, 450 paddlewheel structure, 451 carboxylic adds, 438 trinuclear, 441 oorroles, 874... [Pg.1074]

For example, (CF3)2CH-N=C(Cl-C6H4)N[2,6-Me2C6H3]-SiCl3 4a is obtained from the reaction of the 1,3-diaza-1,3-butadiene with equimolar amounts of HSiCb and DBU. As shown by X-ray structure determination, the amidinate acts as a semi-chelating ligand with a very weak Si-N(2) contact (Fig. 2). [Pg.56]

The general coordination modes of amidinate and guanidinate (R = NR 2) ligands are shown in Scheme 4. Both ligands display a rich coordination chemistry in which both chelating and bridging coordination modes can be achieved. By far the most common coordination mode is the chelating type A. [Pg.186]

The synthesis and characterization of the monomeric amidinato-indium(I) and thallium(I) complexes [Bu C(NAr)2]M[But(NAr(NHAr)] (M = In, Tl Ar = 2,6-Pr2CgH3) have been reported. Both compounds were isolated as pale yellow crystals in 72-74% yield. These complexes, in which the metal center is chelated by the amidinate ligand in an N, j -arene-fashion (Scheme 33), can be considered as isomers of four-membered Group 13 metal(I) carbene analogs. Theoretical studies have compared the relative energies of both isomeric forms of a model compound, In[HC(NPh)2]. ... [Pg.210]


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See also in sourсe #XX -- [ Pg.2 , Pg.203 ]




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Amidinate

Amidinates

Amidination

Amidine ligands

Amidines

Amidins

Chelate ligands

Chelated ligand

Ligands amidinate

Ligands chelation

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