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Terpyridyls

Classic A/-heterocychc ligands, eg, bipyridyl (bipy), terpyridyl, imidazole, pyrazine, phenanthroline, piperazine (including alkyl- and aryl-substituted derivatives), and polypyrazol-l-yl-borates (bis, tris, and tetra), have all been found to coordinate Th(IV) chlorides, perchlorates, and nitrates. The tripodal hydrotris(pyrazolyl)borates, HBPz, have been used to stabilize organometaHic complexes (31). Bis-porphyrin Th(IV) "sandwich" complexes have been... [Pg.37]

The steric crowding introduced in the latter by the four ethyl substituents inhibits nucleophilic attack at platinum, so that complexes of this type tend to undergo substitution by a dissociative mechanism [89]. The complex of the more rigid ligand, 2,2, 2"-terpyridyl, Pt(terpy)Cl+, is found to be about 103 to 104 times more reactive to substitution than the dien analogue this is ascribed to steric strain [90], which is reflected in the short Pt—N bond to the central nitrogen (Pt-N some 0.03 A shorter than the other two Pt-N bonds) and N—Pt—N bond angles of 80-82°). [Pg.208]

With a tridentate ligand Au(terpy)Cl3.H20 has, in fact, AuCl(terpy)2"1" with weakly coordinated chloride and water while Au(terpy)Br(CN)2 has square pyramidal gold(III) the terpyridyl ligand is bidentate, occupying the axial and one basal position [124]. Macrocyclic complexes include the porphyrin complex Au(TPP)Cl (section 4.12.5) cyclam-type macrocyclic ligands have a very high affinity for gold(III) [125],... [Pg.303]

Figure 4.28 Square pyramidal 5-coordination in AuBr(CN)2(terpy) made possible by terpyridyl... Figure 4.28 Square pyramidal 5-coordination in AuBr(CN)2(terpy) made possible by terpyridyl...
The Chemistry of Complexes Containing 2.2 -Bipyridy 1, 1,10-Phenanthroline, or 2.2. 6. 2"-Terpyridyl as Ligands W. R. McWhinnie and J. D. Miller Olefin Complexes of the Transition Metals... [Pg.438]


See other pages where Terpyridyls is mentioned: [Pg.329]    [Pg.356]    [Pg.825]    [Pg.826]    [Pg.28]    [Pg.220]    [Pg.306]    [Pg.377]    [Pg.399]    [Pg.399]    [Pg.408]    [Pg.10]    [Pg.29]    [Pg.77]    [Pg.82]    [Pg.102]    [Pg.102]    [Pg.105]    [Pg.109]    [Pg.109]    [Pg.110]    [Pg.111]    [Pg.115]    [Pg.131]    [Pg.134]    [Pg.155]    [Pg.160]    [Pg.161]    [Pg.176]    [Pg.184]    [Pg.184]    [Pg.185]    [Pg.185]    [Pg.185]    [Pg.185]    [Pg.223]    [Pg.231]    [Pg.232]    [Pg.243]    [Pg.244]    [Pg.11]    [Pg.426]    [Pg.426]    [Pg.8]    [Pg.569]    [Pg.84]   
See also in sourсe #XX -- [ Pg.816 ]




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2,2 ,2"-Terpyridyl

2,2 ,2’’-Terpyridyl metal complexes

2,2 ,2’’-Terpyridyl tris amine

2,2 ,6 ,2"-Terpyridyl oxidation states

2,2 ,6 ,2”-Terpyridyl , as ligand

2,2 -bipyridyl 2,2 :6 ,2"-terpyridyl

Bis-terpyridyl

Chromium complexes 2,2 :6 ,2"-terpyridyl

Cobalt complexes terpyridyl

Ethylenediamine terpyridyl

Lanthanide complexes 2,2 :6 ,2”-terpyridyl

Ligands terpyridyl-containing

Osmium complexes terpyridyl

Platinum® terpyridyl complexes

Ruthenium complexes 2,2 ,2”-Terpyridyl

Sepulchrates terpyridyl

Terpyridyl complexes

Terpyridyl copper complexes

Terpyridyl derivative

Terpyridyl redox properties

Terpyridyl structure

Terpyridyl tris

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