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191.
The phosphorus ylids Ph3PCHR (R = Me, Et, Prn, Pri, Bun, Cl, and OMe), and the ylids Ph3AsCH2, Me2SCH2, and Me2S(O)CH2 react with [Ni(η5-C5H5)Br(PPh3)] at room temperature to give the complexes [Ni(Ph3PCHR)(η5-C5H5(PPh3)] Br, [Ni(Ph3AsCH2)(η5-C5H5)(PPh3)]Br, [Ni(Me2SCH2)(η5-C5H5)(PPh3)]Br and [Ni{Me2S(O)CH2} (η5-C5H5)(PPh3)]Br, respectively. These are readily converted into the corresponding hexafluorophosphate salts on reaction with ammonium hexafluorophosphate. Under more forcing conditions the stabilised ylid Ph3PCHCOPh gives a product believed to be the complex [Ni(Ph3PCHCOPh)2(η5-C5H5)]Br, isolated and characterised as its PF6? salt. 相似文献
192.
Kariuki NN Luo J Maye MM Hassan SA Menard T Naslund HR Lin Y Wang C Engelhard MH Zhong CJ 《Langmuir : the ACS journal of surfaces and colloids》2004,20(25):11240-11246
This paper reports findings of an investigation of the synthesis of monolayer-capped binary gold-silver (AuAg) bimetallic nanoparticles that is aimed at understanding the control factors governing the formation of the bimetallic compositions. The synthesis of alkanethiolate-capped AuAg nanoparticles was carried out using two related synthetic protocols using aqueous sodium borohydride as a reducing agent. One involves a two-phase reduction of AuCl(4)(-), which is dissolved in organic solution, and Ag(+), which is dissolved in aqueous solution. The other protocol involves a two-phase reduction of AuCl(4)(-) and AgBr(2)(-), both of which are dissolved in the same organic solution. AuAg nanoparticles of 2-3 nm core sizes with different compositions in the range of 0-100% Au have been synthesized. The two synthetic routes were compared in terms of bimetallic composition and size properties. Our new findings have allowed us to establish the correlation between synthetic feeding of metals and metal compositions in the bimetallic nanoparticles, which have important implications to the exploration of gold-based bimetallic nanoparticles for constructing sensing and catalytic nanomaterials. 相似文献
193.
Chemistry is described for the fabrication of DNA arrays on gold surfaces. Alkanethiols modified with terminal aldehyde groups are used to prepare a self-assembled monolayer (SAM). The aldehyde groups of the monolayer may be reacted with amine-modified oligonucleotides or other amine-bearing biomolecules to form a Schiff base, which may then be reduced to a stable secondary amine by treatment with sodium cyanoborohydride. The surface modifications and reactions are characterized by polarization modulation Fourier transform infrared reflection absorption spectroscopy (PM-FTIRRAS), and the accessibility, binding specificity, and stability of the DNA-modified surfaces are demonstrated in hybridization experiments. 相似文献
194.
The 13C and proton NMR spectra of six porphyrins bearing the substituent orientation characteristic of the natural “Type-IX” arrangement are reported and assigned. Significant concentration effects in the spectra of the free base porphyrins, together with the broadening of the Cα (and occasionally Cβ) carbon resonances due to NH tautomerism caused a significant loss of data in these spectra. However, the spectra of the corresponding zinc(II) porphyrins (with addition of excess pyrrolidine) show that both these extraneous effects are completely removed to give well-resolved spectra with accurately reproducible chemical shifts. These spectra are assigned and an analysis of the chemical shifts allows the deduction of substituent chemical shift (SCS) parameters for the peripheral substituents at the beta and meso carbons. There is no global effect of these beta substituents, the beta carbon SCS being confined to the immediate pyrrole ring, and the meso carbon SCS to the two adjacent pyrrole rings. The SCS parameters are analyzed and it is shown how they can be used to predict the peripheral and meso carbon chemical shifts of any porphyrin bearing the substituents discussed. 相似文献
195.
Summary A method is described for the combustion of halogen containing organic compounds in milligram quantities in a closed system. It has been found to have greater applicability than existing techniques. After combustion the halogen is determined by an amperometric titration, which permits the determination of Cl–, Br– and I– either singly or in admixture. The accuracy is probably better than existing micro methods for single halides and comparable with these methods for mixed halides.
Zusammenfassung Eine Methode zur Verbrennung von Milligrammengen halogenhaltiger organischer Verbindungen im geschlossenen System wurde beschrieben. Sie hat einen größeren Anwendungsbereich als bisher bekannte Verfahren. Nach der Verbrennung wird das Halogen durch eine amperometrische Titration bestimmt, womit Chlorid, Bromid und Jodid sowohl einzeln wie in Gemischen bestimmt werden können. Die Genauigkeit seheint besser zu sein als bei bekannten Mikromethoden für die Bestimmung einzelner Halogene und etwa gleich gut wie bei Methoden zur Analyse von Halogengemischen.
Résumé On décrit une méthode de combustion en vase clos, des composés organiques contenant des halogènes en quantités de l'ordre du milligramme. Cette méthode a été trouvée comme ayant un domaine d'applications plus grand que celui des techniques existant déjà. Après combustion, l'halogène est dosé par titrage ampérométrique, ce qui permet le dosage de Cl–, Br– et I– isolés ou en mélange. La précision est probablement meilleure que celle des microméthodes existant pour les halogénures isolés et comparable à celle de ces méthodes pour les mélanges d'halogénures.相似文献
196.
Jesik R Abramov V Antipov Y Baldin B Crittenden R Dauwe L Davis C Denisov S Dyshkant A Dzierba A Glebov V Goldberg H Gribushin A Koreshev V Krider J Krinitsyn A Li R Margulies S Marshall T Martin J Mendez H Petrukhin A Sirotenko V Smith P Solomon J Sulanke T Sulyaev R Vaca F Zieminski A Blusk S Bromberg C Chang P Choudhary B Chung W de Barbaro L Dlugosz W Dunlea J Engels E Fanourakis G Ginther G Hartman K Huston J Kapoor V Lirakis C Lobkowicz F Mani S Mansour J Maul A Miller R Oh B Pothier E 《Physical review letters》1995,74(4):495-498
197.
Balest R Cho K Ford WT Lohner M Park H Rankin P Smith JG Alexander JP Bebek C Berger BE Berkelman K Bloom K Browder TE Cassel DG Cho HA Coffman DM Crowcroft DS Dickson M Drell PS Dumas DJ Ehrlich R Elia R Gaidarev P Garcia-Sciveres M Gittelman B Gray SW Hartill DL Heltsley BK Henderson S Jones CD Jones SL Kandaswamy J Katayama N Kim PC Kreinick DL Lee T Liu Y Ludwig GS Masui J Mevissen J Mistry NB Ng CR Nordberg E Patterson JR Peterson D Riley D Soffer A Avery P Freyberger A Lingel K Prescott C 《Physical review letters》1995,75(21):3809-3813
198.
199.
Artuso M Gao M Goldberg M He D Horwitz N Moneti GC Mountain R Muheim F Mukhin Y Playfer S Rozen Y Stone S Xing X Zhu G Bartelt J Csorna SE Egyed Z Jain V Gibaut D Kinoshita K Pomianowski P Barish B Chadha M Chan S Cowen DF Eigen G Miller JS O'Grady C Urheim J Weinstein AJ Würthwein F Asner DM Athanas M Bliss DW Brower WS Masek G Paar HP Gronberg J Korte CM Kutschke R Menary S Morrison RJ Nakanishi S Nelson HN Nelson TK Qiao C Richman JD Roberts D Ryd A Tajima H Witherell MS Balest R Cho K 《Physical review letters》1995,75(5):785-789
200.
McFarland KS Naples D Arroyo CG Auchincloss P de Barbaro P Bazarko AO Bernstein RH Bodek A Bolton T Budd H Conrad J Drucker RB Harris DA Johnson RA Kim JH King BJ Kinnel T Koizumi G Koutsoliotas S Lamm MJ Lefmann WC Marsh W McNulty C Mishra SR Nienaber P Nussbaum M Oreglia MJ Perera L Quintas PZ Romosan A Sakumoto WK Schumm BA Sciulli FJ Seligman WG Shaevitz MH Smith WH Spentzouris P Steiner R Stern EG Vakili M Yang UK 《Physical review letters》1995,75(22):3993-3996