Reversible guest exchange and ferrimagnetism (T(C) = 60.5 K) in a porous cobalt(II)-hydroxide layer structure pillared with trans-1,4-cyclohexanedicarboxylate

The synthesis, characterization, and reversible guest-exchange chemistry of a new porous magnetic material that orders ferrimagnetically at 60.5 K are described. The material, Co(5)(OH)(8)(chdc).4H(2)O (chdc = trans-1,4-cyclohexanedicarboxylate), contains tetrahedral-octahedral-tetrahedral Co(II)-hydroxide layers of composition Co((oct))(3)Co((tet))(2)(OH)(8) that are linked together by bis(unidentate) chdc pillars. Noncoordinated water molecules occupy 1-D channels situated between the chdc pillars. The material remains monocrystalline during dehydration from Co(5)(OH)(8)(chdc).4H(2)O (CDCC.4H(2)O) to Co(5)(OH)(8)(chdc) (CDCC) via an intermediate Co(5)(OH)(8)(chdc).2H(2)O (CDCC.2H(2)O) upon heating or evacuation. In-situ single crystal and powder X-ray diffraction analyses indicate that the interlayer spacing decreases in two steps, each corresponding to the loss of two water molecules per formula unit as determined by thermogravimetry. The single crystal structure of the fully dehydrated material, CDCC, has no void volume due to a tilting of the pillars and 9% decrease of the interlayer spacing with water removal. Exposure of CDCC to air causes rapid rehydration of this material to CDCC.4H(2)O, as determined by single crystal X-ray diffraction, powder X-ray diffraction, thermogravimetry, and vibrational spectroscopy. Both the hydrated and dehydrated forms order magnetically below 60.5 K. The susceptibility data are consistent with ferrimagnetic behavior, and the value of the saturation magnetization at 2 K (ca. 2 micro(B)) is explained by a model of two sublattices, one comprising three octahedral cobalt atoms and another comprising two tetrahedral cobalt atoms. There is an enhanced 2-D correlation within the layer at temperatures just above the Curie temperature, as seen by nonlinearity in the ac susceptibility data and remanence in the isothermal magnetization. The crossover from 2-D to 3-D ordering occurs at T(C). The large anisotropy in the magnetization data on a single crystal suggests either a 2-D Ising or an XY magnet while the critical exponent of 0.25 is in favor of the latter. Both magnetization data in a small field in the ac and dc mode and isothermal magnetization data provide evidence of a further change in behavior at 23 K, which may originate from a reorientation of the moments within the layer. Variation of the pillar and of the guest-exchange chemistry, including the exchange of magnetic guests such as O(2), offers the possibility of tailoring the magnetic properties of this material.     

The synthesis of 1-amino-2-hydroxy- and 2-amino-1-hydroxy-substituted ethylene-1,1-bisphosphonic acids and their N-methylated derivatives

A synthesis of 2-amino-1-hydroxyethylene-1,1-bisphosphonic acid 3 has been developed from N-phthaloylglycine via dimethyl 2-(N-phthaloylamino)acetylphosphonate 1. The preparation of the N-methylated and N,N-dimethylated derivatives 4 and 5 has been achieved by the reaction of 3 with formic acid and formaldehyde. The synthesis of 1-amino-2-hydroxyethylene-1,1-bisphosphonic acid 9 (R=R′=H) and its N-methylated and N,N-dimethylated analogues has been achieved by the reaction of phosphorus trichloride and phosphorous acid with the appropriate O-benzyl protected hydroxyacetamide, followed by catalytic hydrogenolysis of the protecting group.     

Enantiopure bicyclic piperidinones: stereocontrolled conjugate additions leading to substituted piperidinones

The conjugate additions of Reformatsky reagents, organocuprate reagents, and hydroxylamines to a [4.3.0]-bicyclic enelactam derived from 6-oxopipecolic acid have been investigated, and found to be efficient, proceeding with excellent exo-stereocontrol, with the exception of N-benzyl-O-benzylhydroxylamine, which gives predominantly the product of endo-addition. These adducts can be readily converted to substituted piperidinones.     

Probing structure in the polymorphic domain of the L-enantiomer of N-benzoyl-phenylalanine by means of 2D solid-state NMR spectroscopy and DFT calculations

A study of polymorphism using a range of solid-state NMR techniques is presented. We demonstrate the existence of at least six polymorphs in a sample of N-benzoyl-L-phenylalanine. We also present methodology for the characterization of the protonation state, hydrogen bonding, and molecular conformation for the polymorphs, together with results of such a characterization for one of the polymorphs present in our sample. DFT modeling is used to investigate the separate effects hydrogen bonding and molecular conformation have on the chemical shift tensor.     

Polyferredoxin-based electrode materials

Electrochemical oxidation of the hydrosulfide cluster [Fe4S4(SH)4]2- on gold, platinum or vitreous carbon in a methyl cyanide electrolyte leads to the growth of a conducting film. Spectroscopic and other evidence suggests that the film has cubane centres, predominately in the [4Fe4S]3+ oxidation state, which are linked by disulfide ligands to give an anionic array of [Fe4S4(S approximately)4]n- units. X-ray data suggests some long-range order in the electrode material. The polyferredoxin binds redox active cations consistent with an anionic array.     

Establishing the parabolic relationship between reactivity and activity for derivatives and analogues of the duocarmycin and CC-1065 alkylation subunits

The preparation of a novel series of N-aryl CBI derivatives is detailed in which an aryl para substituent could be used to predictably modulate the reactivity of the resulting CC-1065/duocarmycin alkylation subunit analogue (rho = 0.17). The derivatives were found to be exceptionally stable and to exhibit a well-defined relationship between reactivity and cytotoxic potency. When combined with the results of an extensive series of N-acyl CBI analogues and derivatives assembled over the past 15 years, the studies define a fundamental parabolic relationship between reactivity and cytotoxic potency.     

Plasma protein map: an update by microsequencing.

The reference plasma protein map, obtained with immobilized pH gradients in the first dimension of two-dimensional electrophoresis, is presented. By microsequencing, more than 40 polypeptide chains were identified. The new polypeptides and previously known proteins are listed in a table and labeled on the protein map, thus providing an update of the human plasma two-dimensional gel database.     

A 13C and 1H NMR investigation of the bonding in norbornenyl complexes of palladium(II) and platinum(II)

The modes of bonding in several norbornenyl complexes of palladinm(II) and platinum(II) has been investigated by both ¹H and ¹³C NMR spectroscopy. Analysis of internal ¹H¹H, ¹³C¹H, and ¹⁹⁵Pt¹³C coupling constants indicate considerable distortion of the norbornenyl ligand in these complexes relative to organic norbornenes. The nature of this distortion is compatible with a π-homoallylic bonding scheme.     

Self-assembled nanotubes that reversibly bind acetic acid guests

A large bis-urea macrocycle was synthesized and assembled into columnar nanotubes containing a sizable cavity. This purely organic nanotube is held together primarily by hydrogen bonding and yet shows remarkable thermal stability up to 180 degrees C in the presence and absence of acetic acid guest. This enables the nanotube to be used as reusable organic zeolite.     

Rotational spectrum, inversion, and geometry of 2,5-dihydrofuran...ethyne and a generalization about Z...H-C hydrogen bonds

The ground-state rotational spectra of nine isotopomers of a complex formed between 2,5-dihydrofuran and ethyne were recorded with a pulsed-jet, Fourier-transform microwave spectrometer. Rotational and centrifugal distortion constants were obtained for C4H6O...HCCH, C4H6O...DCCH, C4H6O...HCCD, C4H6O...DCCD, [3,4-D2]-C4H6O...HCCH, C4H6O...H13CCH, C4H6O...HC13CH, , and [3(13C]-C4H6O...HCCH. The substituted species were studied in their natural abundances. For the more abundant isotopomers, weak c-type transitions as well as strong a-type transitions were observed. The primary intermolecular binding was shown to consist of a hydrogen bond formed by the ethyne subunit acting as the proton donor and the O atom of 2,5-dihydrofuran as the proton acceptor. The complex has a plane of symmetry that includes the O atom and the ethyne subunit, with a pyramidal configuration at oxygen. A fit of the principal moments of inertia of all nine isotopomers under the assumption of unperturbed 2,5-dihydrofuran and ethyne geometries yielded the values r(O...H)=2.127(8) A, phi=57.8(18) degrees , and theta=16.2(32) degrees, where phi is the angle made by the HCCH subunit at O and theta is the angular deviation of the O...H-C nuclei from collinearity. This geometry is compared with those obtained by ab initio calculations conducted with a range of basis sets and with electron correlation taken into account at the MP2 (M?ller-Plesset second order) level of theory. A small inversion doubling (approximately equal to 20-30 kHz) of c-type transitions, well resolved only for the parent isotopomer and [3HCCH, was attributed to a vibrational motion that inverts the configuration at oxygen. A one-dimensional model for this motion was used with a double minimum potential energy function of the type V(phi)=alphaphi(4)+betaphi(2) to estimate the observed separation DeltaE(01) of the lowest pair (v=0 and v=1) of associated energy levels. The predicted DeltaE(01) had the same magnitude as that deduced from the inversion doubling of the c-type transitions. The geometry of C4H6O...HCCH is compared with those other B...HCCH, where B is vinyl fluoride, oxirane, and thiirane. A rationalization of the angular geometries of various B...HX, where X=F, Cl, Br, or CCH, is presented.