ABSTRACT
The design of new organic-inorganic hybrid ionic materials is of interest for various applications, particularly in the areas of crystal engineering, supramolecular chemistry and materials science. The monohalogenated intermediates 1-(2-chloroethyl)pyridinium chloride, C5H5NCH2CH2Cl(+)·Cl(-), (I'), and 1-(2-bromoethyl)pyridinium bromide, C5H5NCH2CH2Br(+)·Br(-), (II'), and the ionic disubstituted products 1,1'-(ethylene-1,2-diyl)dipyridinium dichloride dihydrate, C12H14N2(2+)·2Cl(-)·2H2O, (I), and 1,1'-(ethylene-1,2-diyl)dipyridinium dibromide, C12H14N2(2+)·2Br(-), (II), have been isolated as powders from the reactions of pyridine with the appropriate 1,2-dihaloethanes. The monohalogenated intermediates (I') and (II') were characterized by multinuclear NMR spectroscopy, while (I) and (II) were structurally characterized using powder X-ray diffraction. Both (I) and (II) crystallize with half the empirical formula in the asymmetric unit in the triclinic space group P-1. The organic 1,1'-(ethylene-1,2-diyl)dipyridinium dications, which display approximate C2h symmetry in both structures, are situated on inversion centres. The components in (I) are linked via intermolecular O-H...Cl, C-H...Cl and C-H...O hydrogen bonds into a three-dimensional framework, while for (II), they are connected via weak intermolecular C-H...Br hydrogen bonds into one-dimensional chains in the [110] direction. The nucleophilic substitution reactions of 1,2-dichloroethane and 1,2-dibromoethane with pyridine have been investigated by ab initio quantum chemical calculations using the 6-31G** basis. In both cases, the reactions occur in two exothermic stages involving consecutive SN2 nucleophilic substitutions. The isolation of the monosubstituted intermediate in each case is strong evidence that the second step is not fast relative to the first.
ABSTRACT
Treatment of the cage compound P6C4(t)Bu4 with M(N(SiMe3)2)2 (M = Ge or Sn) or Pb(C6H3(NMe2)2- 2,6) at room temperature results in their specific insertion into the P-P bond connecting the two 5-membered P3C2(t)Bu2 rings. The products were fully characterised by multinuclear NMR spectroscopy and single crystal X-ray diffraction studies.
Subject(s)
Germanium/chemistry , Lead/chemistry , Organometallic Compounds/chemistry , Organophosphorus Compounds/chemistry , Organotin Compounds/chemistry , Crystallography, X-Ray , Models, Molecular , Molecular Structure , Organometallic Compounds/chemical synthesis , Organophosphorus Compounds/chemical synthesis , Organotin Compounds/chemical synthesis , StereoisomerismABSTRACT
The hexaphosphapentaprismane P(6)C(4)(t)Bu(4) undergoes specific insertion of the zerovalent platinum fragment [Pt(PPh(3))(2)] into the unique P-P bond between the 5-membered rings to afford [Pt(PPh(3))(2)P(6)C(4)(t)Bu(4)]. A similar reaction with the Pt(ii) complexes [{PtCl(2)(PMe(3))}(2)] and [PtCl(2)(eta(4)-COD)] results in both insertion and chlorine migration reactions. The complexes [Pt(PPh(3))(2)P(6)C(4)(t)Bu(4)], trans-[PtCl(PMe(3))P(6)C(4)(t)Bu(4)Cl], cis-,trans-[{PtCl(2)(PMe(3))}micro-{P(6)C(4)(t)Bu(4)}{PtCl(2)(PMe(3))}], [{PtClP(6)C(4)(t)Bu(4)Cl}(2)] and cis-[PtClP(6)C(4)(t)Bu(4)Cl(P(6)C(4)(t)Bu(4))] have been structurally characterized by single crystal X-ray diffraction and multinuclear NMR studies.
Subject(s)
Furans/chemistry , Halogens/chemistry , Heterocyclic Compounds, 4 or More Rings/chemistry , Organophosphorus Compounds/chemistry , Organoplatinum Compounds/chemistry , Bridged-Ring Compounds/chemistry , Crystallography, X-Ray , Magnetic Resonance Spectroscopy , Molecular StructureABSTRACT
Several independent synthetic routes are described leading to the formation of a novel unsaturated tetracyclic phosphorus carbon cage compound tBu4C4P6 (1), which undergoes a light-induced valence isomerization to produce the first hexaphosphapentaprismane cage tBu4C4P6 (2). A second unsaturated isomer tBu4C4P6 (9) of 1 and the bis-[W(CO)5] complex 13 of 1 are stable towards similar isomerization reactions. Another starting material for the synthesis of the hexaphosphapentaprismane cage tBu4C4P6 (2) is the trimeric mercury complex [(tBu4C4P6)Hg]3 (11), which undergoes elimination of mercury to afford the title compound 2. Single-crystal X-ray structural determinations have been carried out on compounds 1, 2, 9, 11, and 13.
