Biomedical subjects

Scott R Wilson

Publications and source records attributed to Scott R Wilson.

27 records · Page 2Linked to original sources

PubMed2003

Three hydrates of the bisphosphonate risedronate, consisting of one molecular and two ionic structures.

Three different hydrates of risedronate were obtained by varying the pH of a solution containing the compound. At the pH values used, the N atom of the pyridine group is protonated and the compounds are zwitterionic. Crystals obtained directly from the synthesis resulted in risedronate monohydrate, or [1-hydroxy-1-phosphono-2-(pyridinium-3-yl)ethyl]phosphonate monohydrate, C(7)H(11)NO(7)P(2).H(2)O, (I), in which just one phosphonate group is negatively charged. Recrystallizations at pH values of 2 and 4 yielded risedronate dihydrate, or sodium [1-hydroxy-2-(pyridinium-3-yl)ethane-1,2-diyl]bis(phosphonate) dihydrate, Na(+).C(7)H(10)NO(7)P(2)(-).2H(2)O, (II). Finally, recrystallizations at pH values of 7 and 8 produced risedronate 2.5-hydrate, or sodium [1-hydroxy-2-(pyridinium-3-yl)ethane-1,2-diyl]bis(phosphonate) 2.5-hydrate, Na(+).C(7)H(10)NO(7)P(2)(-).2.5H(2)O, (III). At these four pH values, both phosphonate groups in (II) and (III) are negatively charged and coordinated to an Na(+) ion. Crystals of (II), i.e. those grown at pH values of 2 and 4, have isomorphous polymeric ion aggregate structures with geminal phosphonate and alcohol groups coordinated to the same Na(+) ion. On the other hand, crystals of (III), i.e. those grown at pH values of 7 and 8, have isomorphism polymeric ion aggregate structures with geminal phosphonate and alcohol groups coordinated to different Na(+) ions.

Alanine↗

PubMed2002

New class of diiron dithiolates related to the Fe-only hydrogenase active site: synthesis and characterization of [Fe2(SR)(2)(CNMe)7]2+.

Electron-rich polyisocyano derivatives Fe(2)(S(2)C(n)H(2n)(CO)(6-x)(CNMe)(x) (x approximately 4) undergo oxidatively induced (FeCp(2)(+)) reaction with additional CNMe to give [Fe(2)(SR)(2)(CNMe)(7)](PF(6))(2), a new class of iron thiolates. Crystallographic characterization established that the 34 e(-) dinuclear core resembles the oxidized (H(2)-binding) form of the active sites of the Fe-only hydrogenases, key features being the face-sharing bioctahedral geometry, the mu-CX ligand, and an Fe-Fe separation of 2.61 A. Oxidation of the phenylthiolate Fe(2)(SPh)(2)(CO)(2)(CNMe)(4) led to mononuclear [Fe(SPh)(CNMe)(5)](PF(6)), which is analogous to [Fe(2)(SR)(2)(CNMe)(10)](PF(6))(2) formed upon treatment of [Fe(2)(S(2)C(3)H(6))(CNMe)(7)](PF(6))(2) with excess CNMe.

Binding Sites↗

PubMed2002

Monosodium [1-hydroxy-2-(1H-imidazol-3-ium-4-yl)ethane-1,1-diyl]bis(phosphonate) tetrahydrate (monosodium isozoledronate).

The title compound, Na(+).C(5)H(9)N(2)O(7)P(2)(-).4H(2)O, is an isomer of zoledronate, a potent bone antiresorptive bisphosphonate drug having significant activity against several parasitic protozoa. The crystal structure of isozoledronate consists of bisphosphonate dimers coordinated by two Na(+) ions. The dimers are held together through an extensive hydrogen-bonding network. The crystals exhibit non-merohedral twinning that roughly superimposes the a and b axes, and inverts the c axis.

Crystallography, X-Ray↗

PubMed2002

Dichloroacetylene is not the precursor to dichlorinated vinylcobaloxime and vinylcobalamin in cobalt catalyzed dechlorination of perchloro- and trichloroethylene.

Vitamin B(12) catalyzes the reductive dechlorination of perchloroethylene (PCE), a process for which vinylcobalamins have been proposed as intermediates. Previous model studies have shown that PCE and trichloroethlylene (TCE) react with cob(I)aloxime to form cis-1,2-dichlorovinylcobaloxime (1). This compound could be formed by nucleophilic vinylic substitution of cob(I)aloxime on TCE or its syn-addition to dichloroacetylene. To evaluate the latter possibility, dichloroacetylene was reacted in this study with cob(I)aloxime. The major product was not complex 1 but a novel cobalt complex, indicating that dichloroacetylene is not involved in the reductive dechorination of PCE catalyzed by cob(I)aloxime. An X-ray structure of the major product was obtained showing an unexpected tricyclic structure in which one of the carbons of dichloroacetylene is a ligand to the metal and the second carbon has formed a C-C bond to one of the oxime carbons. This arrangement connects the axial and equatorial ligands. The cathodic peak potential of this complex is significantly more negative than that of previously characterized chlorinated vinylcobaloximes. Cob(I)alamin also reacts with chloroacetylene to provide cis-chlorovinylcobalamin in analogy to cob(I)aloxime, but it does not provide dichlorinated vinylcobalamins in the reaction with dichloroacetylene. Hence, dichlorinated vinylcobalt complexes detected in the reductive dechlorination of PCE catalyzed by cobaloximes or vitamin B(12) are not derived from a dichloroacetylene intermediate.

Acetylene↗

PubMed2002

New class of ruthenium sulfide clusters: Ru(4)S(6)(PPh(3))(4), Ru(5)S(6)(PPh(3))(5), and Ru(6)S(8)(PPh(3))(6).

Reaction of RuCl(2)(PPh(3))(3) with S(2)(-) sources yields a family of phosphine-containing Ru-S clusters which have been characterized crystallographically and by MALDI-MS. Ru(4)S(6)(PPh(3))(4) (Ru-Ru(av) = 2.94 A) has idealized T(d)() symmetry whereas Ru(6)S(8)(PPh(3))(6) (Ru-Ru(av) = 2.82 A) adopts the idealized O(h)() symmetry characteristic of Chevrel clusters. Ru(5)S(6)(PPh(3))(5) is formally derived by the addition of Ru(PPh(3)) to one face of Ru(4)S(6)(PPh(3))(4). In terms of its M-S connectivity, the Ru(5)S(6) cluster resembles a fragment of the FeMo cluster in nitrogenase.

Journal Article↗

PubMed2002

Systematic assembly of the double molecular boxes: [Cs subset [CpCo(CN)(3)](4)[Cp*Ru](3)] as a tridentate ligand.

Cubic cage compounds composed of Co-CN-Ru linkages have been prepared which illustrate the following features: (i) new motifs for alkali metal ion complexation (i.e., cationic receptors for cations), (ii) a new family of triaza-metalloligands, and (iii) a double box-like cage. The cages are synthesized by the condensation of [CpCo(CN)(3)](-) and [Cp*Ru(NCMe)(3)](+) (cyclopentadienyl, Cp; pentamethylcyclopentadienyl, Cp*) the presence of Cs(+). The species [Cs subset[[CpCo(CN)(3)](4)[Cp*Ru](4)](+) and [Cs subset[[CpCo(CN)(3)](4)[Cp*Ru](3)[Cp*Rh]](2+) illustrate the box-completion reaction Cs subset Co(4)Ru(3) + M (M = Cp*Rh(2+), Cp*Ru(+)). With the naked ion precursors [Na(NCMe)(6)](+) and [Fe(NCMe)(6)](2+), the box-completion reactions afforded [Na[Cs subset[CpCo(CN)(3)](4)[Cp*Ru](3)]](2)](+) and [Fe[Cs subset [CpCo(CN)(3)](4)[Cp*Ru](3)]](2)](2+). These cages provide the first examples, to our knowledge, of the double-box motif.

Bridged-Ring Compounds↗

PubMed2002

Preparative and structural studies on the carbonyl cyanides of iron, manganese, and ruthenium: fundamentals relevant to the hydrogenases.

The reaction of cyanide, carbon monoxide, and ferrous derivatives led to the isolation of three products, trans- and cis-[Fe(CN)(4)(CO)(2)](2)(-) and [Fe(CN)(5)(CO)](3)(-), the first two of which were characterized by single-crystal X-ray diffraction. The new compounds show self-consistent IR, (13)C NMR, and mass spectroscopic properties. The reaction of trans-[Fe(CN)(4)(CO)(2)](2)(-) with Et(4)NCN gives [Fe(CN)(5)(CO)](3)(-) via a first-order (dissociative) pathway. The corresponding cyanation of cis-[Fe(CN)(4)(CO)(2)](2)(-), which is a minor product of the Fe(II)/CN(-)/CO reaction, does not proceed at measurable rates. Methylation of [Fe(CN)(5)(CO)](3)(-) gave exclusively cis-[Fe(CN)(4)(CNMe)(CO)](2)(-), demonstrating the enhanced nucleophilicity of CN(-) trans to CN(-) vs. CN(-) trans to CO. Methylation has an electronic effect similar to that of protonation as determined electrochemically. We also characterized [M(CN)(3)(CO)(3)](n)(-) for Ru (n = 1) and Mn (n = 2) derivatives. The Ru complex, which is new, was prepared by cyanation of a [RuCl(2)(CO)(3)](2) solution.

Carbon Monoxide↗

PubMed2002

Synthesis and characterization of chlorinated alkenylcobaloximes to probe the mechanism of vitamin B(12)-catalyzed dechlorination of priority pollutants.

Vitamin B(12) catalyzes the reductive dechlorination of several ubiquitous pollutants such as perchloroethylene (PCE) and trichloroethylene (TCE). Several mechanisms have been proposed for these transformations, some of which involve the intermediacy of chlorinated vinylcobalamins. To evaluate the currently unknown chemical and physical properties of such species, various chlorinated vinylcobaloxime complexes [cobaloxime = bis(dimethylglyoximato)(pyridine)cobalt(III)] were prepared and characterized. X-ray structures are reported for (cis-1,2-dichloroethenyl)cobaloxime (4), (cis-monochloroethenyl)cobaloxime (5), (alpha-chloroethenyl)cobaloxime (6), and vinylcobaloxime (7), and the reactivities of these isolated complexes were investigated. They were stable in the presence of ethanolic NaBH(4) unless external cobaloximes were added. The cob(I)aloxime formed under the latter conditions promoted the conversion of 4 to 5 and 6, and of 5 and 6 into 7. Mechanistic studies of these transformations are consistent with a pathway in which the conversion of 4 into 5 and 6 takes place via chloroacetylene as an intermediate, and the conversion of 6 to 7 involves vinyl chloride as an intermediate. Cyclic voltammetry on the chlorinated vinylcobaloximes resulted in irreversible reduction waves, with 4 displaying the least negative and 7 the most negative peak potential. These results are discussed in the context of the B(12)-catalyzed reductive dechlorination of PCE and TCE.

Air Pollutants↗

PubMed2002

A functional zeolite analogue assembled from metalloporphyrins.

The assembly of molecular building blocks with metal ions generating microporous network solids has been the focus of intense activity. Because of their potential applications associated with channels and cavities, such materials have been examined for size- and shape-selective catalysis, separations, sensors, molecular recognition and nanoscale reactors. Within this context, assemblies of robust and chemically versatile porphyrin and metalloporphyrin building blocks remain rare. Supramolecular architectures of porphyrin solids based on weak van der Waals interactions, hydrogen bonding and metal-ligand coordination networks have been reported. Although there are frequent allusions to zeolite-like microporosity from crystallography and loss of initial guest solvent molecules, evidence of functional microporous behaviour is scarce. We have demonstrated repeatable sorption-desorption with high selectivity on the basis of size, shape and functional group of the sorbate by a microporous metalloporphyrin solid in analogy to zeolites.

Adsorption↗