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31.
Aija Zirnis Joseph K. Suzuki Donald E. Dickson Robert A. Laitar Albert A. Manian 《Journal of heterocyclic chemistry》1977,14(1):107-112
The synthesis of 7-hydroxy, 8-hydroxy and 7,8-dihydroxy prochlorperazines (3a) and per-phenazines (3b) is reported. The parent ehlorophenothiazines were prepared analogously to previously reported chlorpromazine (3e) metabolite syntheses. The prochlorperazine side chain was introduced in one step using 1-(3-chloropropyl)-4-methylpiperazine and the perphenazine side chain in two steps, first reaction with 1-bromo-3-chloropropane followed by reaction with 1-piperazineethanol. The methoxymethyleneoxy O-proteetive groups were removed under mild conditions using methanolic hydrogen chloride. The preparations of 7-hydroxydesmethylprochlorperazine and 7-hydroxychlorpromazine quaternary methyl iodide are also reported. 相似文献
32.
Mössbauer spectra of the microcrystalline cores of thalassaemic human spleen ferritin and haemosiderin in applied magnetic fields have shown that the magnetic anisotropy dominates over the energy term arising from the net magnetic moments of the microcrystals in the applied field. The spectra have been analysed to give information on the net magnetic moments of the protein cores. 相似文献
33.
Kevin J. Coutinho Ron S. Dickson George A. Koutsantonis Brian W. Skelton Allan H. White Prof. Dr. 《无机化学与普通化学杂志》2008,634(4):669-674
Syntheses of the array of heterobimetallic complexes [(OC)3M(μ‐PPh2)2(μ‐O‐C(CHMe(CH2)2PPh2)RhL], M = Cr, Mo, W, L = tBuNC, are described, extending the previous study of the counterpart array for L = CO. A single crystal X‐ray structure determination is reported for the M = Mo adduct, enabling comparison with its previously reported L = CO counterpart, for which an improved redetermination is also reported. In the present complex the tBuNC ligand is found to be much more weakly bound (Rh‐C 2.026(5) Å) than the carbonyl group it displaces (Rh‐C 1.945(2) Å) with concomitant minor impact on the remainder of the rhodium ambience. 相似文献
34.
Dickson SJ Paterson MJ Willans CE Anderson KM Steed JW 《Chemistry (Weinheim an der Bergstrasse, Germany)》2008,14(24):7296-7305
The synthesis of a series of ruthenium(II) based anion sensors of the type [Ru(eta(6)-C(6)H(4)MeCHMe(2))Cl(L)(2)][BF(4)] (2) is reported in which ligand L represents a series of substituted pyridinylmethyl-amine derivatives. The carbazole based ligand L(3) exhibits a fluorescent intraligand charge-transfer (ILCT) state that is quenched by ligand-to-metal charge transfer (LMCT) upon coordination to ruthenium in the 1:1 complex [Ru(eta(6)-C(6)H(4)MeCHMe(2))Cl(2)(L(3))] (1 c). The 1:2 complex 2 c is fluorescent, however, and acts as a fluorescent anion sensor because of the mixing of an anion-dependent charge-transfer component into the excited state. The 1:2 complexes of type 2 all exhibit interesting low symmetry (1)H NMR spectra that also are a useful handle on anion complexation. The electronic structures of L(3), 1 c and 2 c have been probed by time-dependent DFT calculations. 相似文献
35.
Filby MH Dickson SJ Zaccheroni N Prodi L Bonacchi S Montalti M Paterson MJ Humphries TD Chiorboli C Steed JW 《Journal of the American Chemical Society》2008,130(12):4105-4113
The synthesis, photophysical, and anion-binding properties of a series of di-, tri-, and tetrapodal anion-binding hosts based on aminopyridinium units with pyrenyl reporter groups are described. The ditopic mesitylene-derived calix[4]arene-based host 4 binds strongly to dicarboxylates, particularly malonate, in a 2:1 anion:host ratio but is essentially nonemissive in the presence of all anions except chloride because of intramolecular quenching by the pyridinium units. Addition of chloride results in a conformational change, giving an initial increase in emission assigned to intramolecular excimer formation. Further chloride addition also results in an increase in the intensity of the pyrenyl monomer emission as chloride binding reduces the acceptor ability of the pyridinium groups. This behavior is not exhibited by control compounds 5 and 6, which lack the ditopic geometry and calixarene spacer unit; however, tripodal 6 forms 1:2 anion:host complexes with a range of anions. 相似文献
36.
Christomir Christov Andrew G. Dickson Nancy Moller 《Journal of solution chemistry》2007,36(11-12):1495-1523
In this paper, we describe the development of a thermodynamic model that calculates solute/solvent activities and solid-liquid equilibria in the acidic aluminum system, H-Al3+-Na-K-Cl-H2O, to high molality from 0?° to ≈100?°C. The model incorporates the concentration-dependent, specific interaction equations for aqueous solutions of Pitzer (Activity Coefficients in Electrolyte Solutions, 2nd edn., pp. 75–153, CRC Press, Boca Raton, 1991). Parameterization of this model adds Al3+ specific interactions in the binary Al-Cl-H2O and ternary Al-H-Cl-H2O, Al-Na-Cl-H2O and Al-K-Cl-H2O systems as well as the standard chemical potentials of AlCl3?6H2O(s) and Al(OH)3(s) (gibbsite) in the 0?° to 100?°C range to our variable temperature (0–250?°C) model of acid-base reactions in the H-Na-K-OH-Cl-HSO4-SO4-H2O system (Christov and Moller in Geochim. Cosmochim. Acta 68:1309, 2004). In constructing our aluminum model, we used Emf, osmotic, equilibrium constant and solubility data. New Emf measurements using the cell Pt|H2(g, 101.325 kPa)|HCl(m 1), AlCl3(m 2)|AgCl(s)|Ag|Pt at temperatures ranging from 0 to 45?°C and at total ionic strength ranging from 0.1 to 3 mol?kg?1 are presented. Gibbsite and boehmite, AlOOH(s), solubility data are used in testing the model. Limitations of the model due to data insufficiencies are discussed. 相似文献
37.
Asymmetric ruthenium(II) complexes of a flexible aminomethylpyridine derivative exhibit diastereotopic ligand methylene protons, as measured by NMR spectroscopy; binding of external anions renders these protons equivalent possibly by increasing dynamically averaged symmetry; the amount of anion needed to raise average symmetry correlates to the anion binding constant. 相似文献
38.
Dickson BM 《The Journal of chemical physics》2007,127(6):064106
A noise-space Monte Carlo approach to sampling reactive Langevin trajectories is introduced and compared to a configuration based approach. The noise sampling is shown to overcome the slow relaxation of the configuration based method. Furthermore, the noise sampling is shown to sample multiple pathways with the correct probabilities without any additional work being required formally or algorithmically. The path sampling proceeds without any introduction of fictitious interactions and includes only the parameters appearing in Langevin's equation. 相似文献
39.
Swarna A. Gamage Julie A. Spicer Kit Y. Tsang Patrick D. O'Connor Jack U. Flanagan Woo‐Jeong Lee James M. J. Dickson Peter R. Shepherd William A. Denny Gordon W. Rewcastle 《化学:亚洲杂志》2019,14(8):1249-1261
Using a scaffold‐hopping approach, imidazo[1,2‐a]pyridine analogues of the ZSTK474 (benzimidazole) class of phosphatidylinositol 3‐kinase (PI3K) inhibitors have been synthesized for biological evaluation. Compounds were prepared using a heteroaryl Heck reaction procedure, involving the palladium‐catalysed coupling of 2‐(difluoromethyl)imidazo[1,2‐a]pyridines with chloro, iodo or trifluoromethanesulfonyloxy (trifloxy) substituted 1,3,5‐triazines or pyrimidines, with the iodo intermediates being preferred in terms of higher yields and milder reaction conditions. The new compounds maintain the PI3K isoform selectivity of their benzimidazole analogues, but in general show less potency. 相似文献
40.
D.P.E. Dickson 《Hyperfine Interactions》1998,111(1-4):171-177
Biological systems can be used both to explore the properties of and to provide novel examples of nanophase magnetic materials. The Mössbauer spectroscopic measurements of the iron-storage protein ferritin and its derivatives, discussed in this paper, provide examples of both these aspects. 相似文献