A novel porous carbon based on diatomaceous earth.
The production and characterisation of a carbon negative of diatomaceous earth which has a highly intricate and novel porous structure.
Biomedical subjects
Publications and source records attributed to S M Holmes.
The production and characterisation of a carbon negative of diatomaceous earth which has a highly intricate and novel porous structure.
A method for the production of mesoporous carbon, with metal particles encapsulated in the walls to prevent leaching, is demonstrated by the synthesis of a cobalt containing CMK1 structure.
The development of low cost hierarchical porous materials based upon the zeolitisation of diatomaceous earth for fluid waste benification is described. Two preparative approaches invole: first, using the diatom as a support for zeolite nanocrystals; second, direct pseudomorphic transformation of the diatom into a zeolite. These hierarchical porous materials are potentially useful for important industrial processes in ion-exchange, catalysis and waste benefication.
Treatment of NaW2Cl7(THF)5 with 4 equiv of (t)Bu3SiNHLi afforded the C2 W(III) dimer [((t)Bu3SiNH)2WCl]2 (1, d(W triple bond W) = 2.337(2) A), which is a rare, primary amide M2X4Y2 species. Its degradation provided evidence of NH bond activation by the ditungsten bond. Addition of 2 equiv of (t)Bu3SiNHLi or TlOSi(t)Bu3 to 1 yielded H2 and hydride ((t)Bu3SiN)2((t)Bu3SiNH)WH (2, d(WH) = 1.67(3) A) or ((t)Bu3SiN)2((t)Bu3SiO)WH (3). Thermolysis (60 degrees C, 16 h) of 1 in py gave ((t)Bu3SiN)2WHCl(py) (4-py, 40-50%), ((t)Bu3SiN)2WCl2(py) (6-py, 10%), and ((t)Bu3SiN)2HW(mu-Cl)(mu-H)2W(NSi(t)Bu3)py2 (5-py2, 5%), whereas thermolysis in DME produced ((t)Bu3SiN)2WCl(OMe) (7, 30%), ((t)Bu3SiN)2WCl2 (6, 20%), and ((t)Bu3SiN)2HW(mu-Cl)(mu-H)2W(NSi(t)Bu3)DME (5-DME, 3%). Compound 7 was independently produced via thermolysis of 4-py and DME (-MeOEt, -py), and THF and ethylene oxide addition to hydride 2 gave ((t)Bu3SiN)2((t)Bu3SiNH)WO(n)Bu (8) and ((t)Bu3SiN)2((t)Bu3SiNH)WOEt (9), respectively. Dichloride 6 was isolated from SnCl4 treatment of 1 with the loss of H2. Sequential NH bond activations by the W2 core lead to "((t)Bu3SiN)2WHCl" (4) and subsequent thermal degradation products. Thermolysis of 1 in the presence of H2C=CH(t)Bu and PhC triple bond CPh trapped 4 and generated ((t)Bu3SiN)2W((neo)Hex)Cl (10) and a approximately 6:1 mixture of ((t)Bu3SiN)2WCl(cis-CPh=CPhH) (11-cis) and ((t)Bu(3)SiN)2WCl(trans-CPh=CPhH) (11-trans), respectively. Thermolysis of the latter mixture afforded ((t)Bu3SiNH)((t)Bu3SiN)WCl(eta2-PhCCPh) (12) as the major constituent. Alkylation of 1 with MeMgBr produced ((t)Bu3SiN)2W(CH3)2 (13), as did addition of 2 equiv of MeMgBr to 6. X-ray crystal structure determinations of 1, 2, 5-py2, 6-py, 11-trans, and 12 confirmed spectroscopic identifications. A general mechanism that features a sequence of NH activations to generate 4, followed by chloride metathesis, olefin insertion, etc., explains the formation of all products.
Potentiometric investigations using pressed zeolite discs are reported. Potential measurements have been performed in non-aqueous solutions--this is the first report, to our knowledge, of potentiometric detection of ions in non-aqueous media with zeolite materials. Nernstian behaviour is also displayed in aqueous solutions for ions that are only able to penetrate a fraction of the internal volume of the zeolite employed.
The silicalite-modified water/organic interface represents a novel system, which is of potential utility for electroanalytical studies. As a means of investigating the analytical potential of this interface the facilitated transfer of various alkali and alkaline earth metal ions have been investigated using voltammetric methods. Additionally, the size selective transfer of tetraalkylammonium ions across this modified interface has been studied and a possible adsorption process that may be a step in the overall transfer has been identified.
A Salmonella typhi abscess within a craniopharyngioma in a 28-year-old woman is reported. CT and MRI demonstration of cerebral edema adjacent to the tumor suggested an atypical presentation of craniopharyngioma.
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An unusual case of an intrasellar schwannoma radiographically simulating a pituitary tumor is reported. The literature on unusual intracranial locations of schwannomas and their possible origin is discussed.
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