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51.
Arun Kumar NS Prashanth Shivappa Adarakatti Ashoka S Pandurangappa Malingappa 《Journal of Solid State Electrochemistry》2018,22(6):1711-1719
A simple strategy has been proposed to quantify Zn2+ ions using CeO2 nanoparticle-modified glassy carbon electrode. The CeO2 nanoparticles were prepared by sucrose-nitrate decomposition method, and it was characterized by X-ray diffraction (XRD), FT-IR, TEM, and surface area analyzer. The synthesized CeO2 nanoparticles were used as modifier molecules as a thin film on glassy carbon electrode (GCE) in the trace level quantification of Zn2+ by using cyclic voltammetry (CV) and differential pulse anodic stripping voltammetry (DPASV) techniques. The fabricated sensor exhibited a good analytical response towards Zn2+ ions. The modified electrode showed a wide linearity in the concentration range 20–380 μg L?1 with a limit of detection 0.36 μg L?1. The proposed electrochemical sensor was successfully applied to trace level Zn2+ quantification from real sample matrices. 相似文献
52.
Ramachandra S. Hosmane Benjamin B. Lim Upali Siriwardane Narayan S. Hosmane 《Journal of chemical crystallography》1991,21(3):353-356
The title compound (IV) was isolated as a by-product during the course of purification of 4-nitroimidazol-5-(N-methyl)hydrazide (II) by silica gel flash chromatography, employing chloroform-acetone (4:1) as the eluting solvent. The crystals are monoclinic, space groupP21/c,a=7.425(1),b=13.615(2),c=10.359(2) Å,=97.66(1)°,d
caled=1.44 g cm–3, (MoK)=1.06 mm–1,T=298 K. The number of unique reflections=2401, reflections withI3 (I)=1773;R=0.051,R
w
=0.061. The bond distances inIV are: N-N, 1.419(3); N-C(=0), 1.359(3); N(H)-C(CH3), 1.457(3); N(C)-C(CH3), 1.501(3); N=C, 1.316(3); C=C, 1.368(3), N-C(=N), 1.353(3); N-C(=C), 1.367(2) Å. 相似文献
53.
Diazomethane and ethyl diazoacetate are highly reactive and highly versatile synthetic reagents that undergo numerous related reactions. However, while the former is highly dangerous because of its toxicity and explosive behavior; the latter is much more benign. This is usually ascribed to resonance stabilization in ethyl diazoacetate involving an extra carbonyl group that is absent in diazomethane, cf. $$\begin{gathered} {\text{EtOOC}}---{\text{CH}} = {\rm N}^ + = {\rm N}^ - \leftrightarrow {\rm E}{\text{tOOC}}---{\text{CH}}^ - ---{\text{N}}^{\text{ + }} \equiv {\text{N}} \leftrightarrow {\text{EtOC(O}}^ - {\text{)}} = {\text{CH}}---{\text{N}}^{\text{ + }} \equiv {\rm N} \hfill \\ {\text{CH}}_{\text{2}} = {\rm N}^ + = {\rm N}^ - \leftrightarrow {\text{CH}}_{\text{2}}^ - ---{\text{N}}^{\text{ + }} \equiv {\rm N} \hfill \\ \end{gathered}$$ The additional resonance stabilization is derived using a recent literature measurement of the enthalpy of an ethyl diazoacetate/aldehyde reaction, key enthalpies of formation, also from the literature, and some simplifying assumptions. The resonance stabilization is deduced to be but 16 kJ/mol, merely 4 kcal/mol. But, oh how grateful we are for this! 相似文献
54.
Adams L Hosmane SN Eklund JE Wang J Hosmane NS 《Journal of the American Chemical Society》2002,124(25):7292-7293
Boron-10 enriched boric acid, H310BO3, was converted to the corresponding sodium borohydride, Na10BH4, in essentially quantitative yields, by using slightly modified literature methods involving the formation of butyl borate, (n-OBu)310B, first and then reacting it with NaH in mineral oil. The oxidation reaction of Na10BH4 with I2 in diglyme and subsequent addition/purification in dioxane gave Na[10B3H8]0.3(C4H8O2) that reacted further with NiCl2 in either anhydrous benzene or heavy mineral oil at 110 degrees C to produce the corresponding 10B5H9 as the first isolated 10B-enriched liquid boron hydride in a laboratory environment. Treatment of this 10B5H9 with NaH or t-BuLi in 2:1 molar ratio underwent a cage expansion reaction to produce the [M]10B9H14 that undergoes a redox reaction in situ with anhydrous NiCl2 in n-hexane to yield the corresponding fused cage anti-10B18H22 as the only solid borane product in 42% yield, thus establishing new synthetic routes for the preparation of 10B-enriched polyhedral boranes. 相似文献
55.
56.
The use of pentafluorophenol as a superior reagent for heterocyclic condensations, where other traditional condensing agents such as DCC and CDI failed, has been demonstrated. 相似文献
57.
Satapathy R Dash BP Bode BP Byczynski EA Hosmane SN Bux S Hosmane NS 《Dalton transactions (Cambridge, England : 2003)》2012,41(29):8982-8988
A series of carborane-appended 5-thio-D-glucopyranose (5-TDGP) derivatives containing one to two 5-TDGP moieties were synthesized via click cycloaddition reaction as well as following the traditional methods. Among the carboranyl-5-TDGP derivatives, the decapitated nido-carboranyl derivative 18 was found to be highly water-soluble and therefore its preliminary biodistribution study was conducted. A comparative biological evaluation of 18 versus its carboranyl-D-glucopyranose analog 19 with human hepatocellular carcinoma cells (SK-Hep1) indicated 5-TDGP to be a better boron carrier than normal D-glucopyranose. The carboranyl-5-TDGP 18 showed a nearly two fold increase in cellular boron accumulation than carboranyl-D-glucopyranose analog 19 over a period of 2 h. The accumulation of both 18 and 19 was found to occur in a temperature dependent manner. The higher accumulation of 18 suggested excellent promise for it to be a candidate for further evaluation as a future BNCT agent. 相似文献
58.
Stewart W. Schneller Jiann-Kuan Luo Ramachandra S. Hosmane Rainer H. DÚrrfeld 《Journal of heterocyclic chemistry》1984,21(4):1153-1155
The synthesis of 1-methyl- ( 1a ) and 1-benzyl-6-amino-1H-pyrrolo[3,2-c]pyridin-4(5H)-one ( 1b ) from the appropriate N-alkylaminoacetaldehyde is described. These provide examples of a synthetic procedure that can be used to prepare 1-substituted 6-amino-1H-pyrrolo[3,2-c]pyridin-4(5H)-ones wherein the N-1 substituent is regiospecifically placed. 相似文献
59.
Narayan S. Hosmane Zhu Yinghuai John A. Maguire 《Journal of organometallic chemistry》2009,694(11):1690-553
An account of the current research carried out in our laboratories is presented. Included is the incorporation of several group 14 elements into charge-compensated carboranes. These species present a bonding pattern not found in other main group carboranes. In addition to our continuing studies of the syntheses and structures of organometallic compounds, the use of these compounds as catalysts and catalyst precursors has been investigated. The isotopic exchange reactions between 10B enriched boron hydrides with naturally abundant boranes catalyzed by Ru(0) nanoparticles has been studied. The Ru(0) nanoparticles were obtained by the reduction of [CpRuCp∗RuCp∗]PF6 (Cp∗ = C5Me5) with hydrogen and stabilized by the ionic liquid trihexyltetradecylphosphonium dodecylbenzenesulfonate [THTdP][DBS]. This was found to be an excellent, long lived catalyst for the exchange reaction of B-10 enriched diborane and naturally abundant decaborane(14). Other approaches to the production and use of nano-metal catalysts have also been explored. The reduction of the iridium carborane, (PPh3)2IrH(7,8-C2B9H11) with hydrogen in the presence of trihexyltetradecylphosphonium methylsulfonate, [THTdP][MS], produced an Ir(0) nanoparticles that catalyzed the phenylborolation as did our Ir(sal = N-R = salicylaldiminato; COD = cyclooctadiene complex. Progress in the use of single wall carbon nanotubes (SWCNT) as boron delivery agents was also discussed. 相似文献
60.