“…The Mg−O distances (1.96(1) Å average) in 14 are significantly shorter (1.96(1) Å in 12 vs 2.04(1) Å in 1 ). The P−O distances (1.48(1) Å average) are similar to those observed in other HMPA complexes, and the slight deviation from linearity of the Mg−O−P angles is not unusual and has been observed in other HMPA metal complexes. 5 Thermal ellipsoid plot (30%) of 14 showing the disorder in one of the (Me 2 N 3 )PO solvating molecules. Only oxygens and ipso-carbon atoms are shown for three of the (Me 2 N) 3 PO and three of the phenyl donors.…”
Imide transfer properties of ((THF)MgNPh)(6) (1) and the synthesis of the related species {(THF)MgN(1-naphthyl)}(6).2.25THF (2), via the reaction of dibutylmagnesium with H(2)N(1-naphthyl), in a THF/heptane mixture are described. Treatment of 1 with Ph(2)CO, 4-Me(2)NC(6)H(4)NO, t-BuNBr(2) (3), PCl(3), or MesPCl(2) (Mes = 2,4,6-Me(3)C(6)H(2)-) leads to the isolation of Ph(2)CNPh (4), 4-Me(2)NC(6)H(4)NNPh (5), t-BuNNPh (6), (PhNPCl)(2) (7), or (MesPNPh)(2) (8) in moderate yield. Reaction between 1 and GeCl(2).dioxane, SnCl(2), or PbCl(2) affords the M(4)N(4) (M = Ge, Sn, Pb) cubane imide derivative (GeNPh)(4) (9), [(SnNPh)(4).{MgCl(2)(THF)(4)}](infinity) (10), (SnNPh)(4).0.5PhMe (11), or (PbNPh)(4).0.5PhMe (12). Interaction of 1 with Ph(3)PO, (Me(2)N)(3)PO, or Ph(2)SO furnishes the complex (Ph(3)POMgNPh)(6) (13), {(Me(2)N)(3)POMgNPh}(6).2PhMe (14), or (Ph(2)SOMgNPh)(6) (15). The addition of 3 equiv of MgBr(2) to 1 gives 1.5 equiv of ((THF)Mg)(6)(NPh)(4)Br(4) (16) in quantitative yield, whereas treatment of 16 with 4 equiv of 1,4-dioxane is an alternative synthetic route to 1. Compounds 2, 3, 9, 10, and 14 were characterized by X-ray crystallography. The reactions demonstrate that 1 is a versatile and useful reagent for the synthesis of a variety of main group imides. Crystal data at 130 K with Mo Kalpha (lambda = 0.710 73 Å) radiation for 3 or Cu Kalpha (lambda = 1.541 78 Å) radiation for 2, 9, 10, and 14: 2, C(93)H(108)Mg(6)N(6)O(7.25), a = 28.101(7) Å, b = 35.851(7) Å, c = 36.816(7) Å, Z = 2, space group Fddd, R = 0.068 for 3500 (I > 2sigma(I)) data; 3, C(4)H(9)Br(2)N, a = 6.682(2) Å, b = 10.834(3) Å, c = 11.080(3) Å, alpha = 66.25(2) degrees, beta = 89.88(2) degrees, gamma = 82.53(2) degrees, Z = 4, space group P&onemacr;, R = 0.038 for 2043 (I > 2sigma(I)) data; 9, C(24)H(20)Ge(4)N(4), a = 10.749(2) Å, b = 12.358(3) Å, c = 35.818(7) Å, Z = 8, space group Pbca, R = 0.040 for 2981 (I > 2sigma(I)) data; 10, C(40)H(52)Cl(2)MgN(4)O(4)Sn(4), a = 12.770(3) Å, b = 13.554(3) Å, c = 25.839(5) Å, Z = 4, space group P2(1)2(1)2(1), R = 0.040 for (I > 2sigma(I)) data; 14, C(86)H(154)Mg(6)N(4)O(6)P(6), a = 22.478(4) Å, b = 16.339(3) Å, c = 29.387(6) Å, Z = 4, space group Pbcn, R = 0.081 for 4696 (I >2sigma(I)) data.
“…The Mg−O distances (1.96(1) Å average) in 14 are significantly shorter (1.96(1) Å in 12 vs 2.04(1) Å in 1 ). The P−O distances (1.48(1) Å average) are similar to those observed in other HMPA complexes, and the slight deviation from linearity of the Mg−O−P angles is not unusual and has been observed in other HMPA metal complexes. 5 Thermal ellipsoid plot (30%) of 14 showing the disorder in one of the (Me 2 N 3 )PO solvating molecules. Only oxygens and ipso-carbon atoms are shown for three of the (Me 2 N) 3 PO and three of the phenyl donors.…”
Imide transfer properties of ((THF)MgNPh)(6) (1) and the synthesis of the related species {(THF)MgN(1-naphthyl)}(6).2.25THF (2), via the reaction of dibutylmagnesium with H(2)N(1-naphthyl), in a THF/heptane mixture are described. Treatment of 1 with Ph(2)CO, 4-Me(2)NC(6)H(4)NO, t-BuNBr(2) (3), PCl(3), or MesPCl(2) (Mes = 2,4,6-Me(3)C(6)H(2)-) leads to the isolation of Ph(2)CNPh (4), 4-Me(2)NC(6)H(4)NNPh (5), t-BuNNPh (6), (PhNPCl)(2) (7), or (MesPNPh)(2) (8) in moderate yield. Reaction between 1 and GeCl(2).dioxane, SnCl(2), or PbCl(2) affords the M(4)N(4) (M = Ge, Sn, Pb) cubane imide derivative (GeNPh)(4) (9), [(SnNPh)(4).{MgCl(2)(THF)(4)}](infinity) (10), (SnNPh)(4).0.5PhMe (11), or (PbNPh)(4).0.5PhMe (12). Interaction of 1 with Ph(3)PO, (Me(2)N)(3)PO, or Ph(2)SO furnishes the complex (Ph(3)POMgNPh)(6) (13), {(Me(2)N)(3)POMgNPh}(6).2PhMe (14), or (Ph(2)SOMgNPh)(6) (15). The addition of 3 equiv of MgBr(2) to 1 gives 1.5 equiv of ((THF)Mg)(6)(NPh)(4)Br(4) (16) in quantitative yield, whereas treatment of 16 with 4 equiv of 1,4-dioxane is an alternative synthetic route to 1. Compounds 2, 3, 9, 10, and 14 were characterized by X-ray crystallography. The reactions demonstrate that 1 is a versatile and useful reagent for the synthesis of a variety of main group imides. Crystal data at 130 K with Mo Kalpha (lambda = 0.710 73 Å) radiation for 3 or Cu Kalpha (lambda = 1.541 78 Å) radiation for 2, 9, 10, and 14: 2, C(93)H(108)Mg(6)N(6)O(7.25), a = 28.101(7) Å, b = 35.851(7) Å, c = 36.816(7) Å, Z = 2, space group Fddd, R = 0.068 for 3500 (I > 2sigma(I)) data; 3, C(4)H(9)Br(2)N, a = 6.682(2) Å, b = 10.834(3) Å, c = 11.080(3) Å, alpha = 66.25(2) degrees, beta = 89.88(2) degrees, gamma = 82.53(2) degrees, Z = 4, space group P&onemacr;, R = 0.038 for 2043 (I > 2sigma(I)) data; 9, C(24)H(20)Ge(4)N(4), a = 10.749(2) Å, b = 12.358(3) Å, c = 35.818(7) Å, Z = 8, space group Pbca, R = 0.040 for 2981 (I > 2sigma(I)) data; 10, C(40)H(52)Cl(2)MgN(4)O(4)Sn(4), a = 12.770(3) Å, b = 13.554(3) Å, c = 25.839(5) Å, Z = 4, space group P2(1)2(1)2(1), R = 0.040 for (I > 2sigma(I)) data; 14, C(86)H(154)Mg(6)N(4)O(6)P(6), a = 22.478(4) Å, b = 16.339(3) Å, c = 29.387(6) Å, Z = 4, space group Pbcn, R = 0.081 for 4696 (I >2sigma(I)) data.
“…There are numerous examples of hexamethylphosphoramide coordination complexes (Sinha et al, 1982;Herrmann et al, 1996;Bombieri et al, 2001;Sü ss-Fink et al, 2004). We present here the structure of the title compound, (I).…”
In the title compound, [MnCl2(C6H18N3OP)], the MnII atom, on a twofold rotation axis, is bonded to two O atoms from two symmetry‐related hexamethylphosphosphoramide (HMPA) ligands and two Cl atoms in a distorted tetrahedral configuration.
“…The high degree of polarization of the P=O bond promotes the formation of strong coordination bonds with metal ions, which leads to the noticeable shifts of the vibrational bands. Coordination of the HMPA molecule to the uranyl ion leads to a decrease of ν(PO) and an increase of ν(PN) and δ(NPN) in the spectrum of complex 1 as compared to the uncoordinated molecule , …”
Behavior of UVI, NpVI and PuVI in water‐acetonitrile solutions was studied spectrophotometrically with the successive addition of the polar organic ligands (dimethyl sulfoxide or hexamethylphosphoric triamide) and the NCS– ion. The detected spectral effects – changes in the absorption intensity, bathochromic shifts in the absorption bands, the absence of isosbestic points, a change in the color of the solution – indicate complex competitive processes occurring in the studied solutions. In the case of NpVI, its partial reduction to NpIV by NCS– ion is observed. Solid UVI complex, [UO2(HMPA)2(NCS)2], was isolated, its crystal structure was determined using X‐ray diffraction. In contrast to known AnO22+ compounds with the NCS– ion, this complex exhibits tetragonal bipyramidal environment of the U atom. [UO2(HMPA)2(NCS)2] is also characterized by UV/Vis, IR and luminescence spectroscopy.
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