2005
DOI: 10.1016/j.poly.2004.08.027
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The synthesis and lanthanide coordination chemistry of 2,6-bis[(dicyclohexyl)phosphino-methyl]pyridine N,P,P′-trioxide

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Cited by 29 publications
(33 citation statements)
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“…A view of the molecular structure is shown in Figure 10, and selected bond lengths are listed in Table 4. As found with 2, the initially isolated 1:1 complex transforms upon crystallization to a 2:1 complex with the composition, [Pr (5) [11][12][13][14][15][16][17][18][19][20][21][22][23][24]. The placement of pyridine and 1-methylpyrazole at the weaker end of the series derives from the relatively softer character of N atom donors.…”
Section: Attempts To Crystallize [Eu(5)(no 3 ) 3 ](H 2 O) From a Varimentioning
confidence: 89%
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“…A view of the molecular structure is shown in Figure 10, and selected bond lengths are listed in Table 4. As found with 2, the initially isolated 1:1 complex transforms upon crystallization to a 2:1 complex with the composition, [Pr (5) [11][12][13][14][15][16][17][18][19][20][21][22][23][24]. The placement of pyridine and 1-methylpyrazole at the weaker end of the series derives from the relatively softer character of N atom donors.…”
Section: Attempts To Crystallize [Eu(5)(no 3 ) 3 ](H 2 O) From a Varimentioning
confidence: 89%
“…For example, the tris-heterocyclic ligand, 2,2':6',2''-terpyridine (terpy), and its numerous derivatives represent one of the most widely investigated classes of chelating ligands used in coordination chemistry [1][2][3][4][5]. Another widely studied class of tris-heterocyclic ligands is the 2,6-In recent contributions we have described several new multidentate phosphine oxide ligands based upon pyridine and pyridine N-oxide platforms including ligands of types E-I, as shown in Figure 1, and their coordination chemistry with f-element ions has proven to be interesting [11][12][13][14][15][16][17][18][19][20][21][22][23][24]. In particular, the Noxide ligands, E and G (designated as NOPO) and I (designated as NOPOPO) appear to bind more effectively with lanthanide [Ln(III)] cations than their pyridine analogs F and H, and the more flexible ligands of types G and I coordinate more strongly than ligands of type E despite the larger chelate ring ray diffraction methods.…”
Section: Introductionmentioning
confidence: 99%
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“…4 The single crystal X-ray structures and solution properties of pentagonal 5 bipyramidal complexes [Ln(H 2 O) 5 a b s t r a c t 24 The products of the reactions of tricyclohexlyphosphine oxide, Cy 3 PO = L, with lanthanide chlorides 25 (Ln = La, Dy, Er, Yb) have been investigated by solution NMR spectroscopy and single crystal X-ray crys- 26 tallography (Dy, Er). The structures of the complexes are based on a pentagonal bipyramidal arrangement 27 around the central Ln 3+ ion with two Cy 3 PO in axial positions and five water molecules in the equatorial 28 plane with molecular formulae LnL n (H 2 O) 5 ÁLÁ3ClÁH 2 OÁEtOH.…”
mentioning
confidence: 99%
“…We have also reported that 2-(methylphosphine oxide) and 2,6-bis-(methylphosphine oxide) substituted pyridines 5, 6 and pyridine N-oxides 7, 8 can be prepared. The latter two ligand types act as especially strong chelating ligands toward lanthanide and actinide ions despite the fact that the chelate rings contain seven atoms [7][8][9][10][11][12][13][14][15][16][17][18]. Indeed, representatives of the ligand 8 have proven to be very effective liquid-liquid extractants for trivalent lanthanide and actinide ions [19][20][21].…”
Section: Introductionmentioning
confidence: 99%