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71.
A Functionalized Ag2S Molecular Architecture: Facile Assembly of the Atomically Precise Ferrocene‐Decorated Nanocluster [Ag74S19(dppp)6(fc(C{O}OCH2CH2S)2)18] 下载免费PDF全文
Yiyi Liu Bahareh Khalili Najafabadi Mahmood Azizpoor Fard Prof. Dr. John F. Corrigan 《Angewandte Chemie (International ed. in English)》2015,54(16):4832-4835
A ferrocene‐based dithiol 1,1′‐[fc(C{O}OCH2CH2SH)2] has been prepared and treated with a AgI salt to form the stable dithiolate compound [fc(C{O}OCH2CH2SAg)2]n (fc=[Fe(η5‐C5H4)2]). This is used as a reagent for the preparation of the nanocluster [Ag74S19(dppp)6(fc(C{O}OCH2CH2S)2)18] which was obtained in good yield (dppp=1,3‐bis(diphenylphosphino)propane). 相似文献
72.
Zal U��yun Wan Mahmood Che Abd Rahim Mohamed Zaharudin Ahmad Abdul Kadir Ishak 《Journal of Radioanalytical and Nuclear Chemistry》2011,287(1):255-260
A total of eight sediment cores with 50 cm length were taken in the Sabah and Sarawak coastal waters using a gravity corer in 2004 to estimate sedimentation rates using four mathematical models of CIC, Shukla-CIC, CRS and ADE. The average of sedimentation rate ranged from 0.24 to 0.48 cm year?1, which is calculated based on the vertical profile of 210Pbex in sediment core. The finding also showed that the sedimentation rates derived from four models were generally shown in good agreement with similar or comparable value at some stations. However, based on statistical analysis of paired sample t-test indicated that CIC model was the most accurate, reliable and suitable technique to determine the sedimentation rate in the coastal area. 相似文献
73.
Mei-Wo Yii Zal U’yun Wan Mahmood 《Journal of Radioanalytical and Nuclear Chemistry》2011,289(3):819-833
This study with sampling expeditions of marine sediment, seawater and biota were performed at 30 stations within Malaysian
Exclusive Economic Zone (EEZ). A total of >400 samples were collected to determine the activity concentration of anthropogenic
radionuclides (239+240Pu, 137Cs) and their activity ratio (239+240Pu/137Cs) in sediments, seawater and biota. The purpose of this study was to determine the concentration levels for these radionuclides
and to evaluate any occurrence of radioactive contamination. Sediment cores were obtained using multicorer device, while water
samples via co-precipitation techniques and biota was purchased from local fishermen. The activity concentrations of 239+240Pu in sediment, seawater and biota were ranged 0.21–0.45 Bq/kg dry wt., 2.33–7.95 mBq/m3 and <0.008 Bq/kg fresh wt., respectively. Meanwhile, the values of 137Cs were ranged <1.00–2.71 Bq/kg dry wt. in sediment, 3.40–5.89 Bq/m3 in seawater and <0.05–0.41 Bq/kg fresh wt. in biota, respectively. Activity ratios of 239+240Pu to 137Cs obtained seem to confirm that these artificial radioactivities were mainly due to global nuclear fallout. 相似文献
74.
Back Cover: New Polydentate Trimethylsilyl Chalcogenide Reagents for the Assembly of Polyferrocenyl Architectures (Chem. Eur. J. 23/2014) 下载免费PDF全文
75.
Dr. Oliver Guillermet Dr. Ather Mahmood Dr. Jianshu Yang Dr. Jorge Echeverria Judicael Jeannoutot Dr. Sebastien Gauthier Dr. Christian Joachim Dr. Frederic Chérioux Prof. Dr. Frank Palmino 《Chemphyschem》2014,15(2):271-275
Thermally activated rotation of single molecules adsorbed on a silicon‐based surface between 77 and 150 K has been successfully achieved. This remarkable phenomenon relies on a nanoporous supramolecular network, which acts as a template to seed periodic molecule rotors on the surface. Thermal activation of rotation has been demonstrated by STM experiments and confirmed by theoretical calculations. 相似文献
76.
Inside Cover: Seeding Molecular Rotators on a Passivated Silicon Surface (ChemPhysChem 2/2014) 下载免费PDF全文
77.
Synthesis,Characterization, and Photoluminescence Properties of Silver(I) Metal‐Organic Polymers with Nanochannels Based on 2‐Sulfoterephthalic Acid and Di(pyridin‐2‐yl)amine Ligands 下载免费PDF全文
Hui Huang Mahmood Payehghadr Jie Wang Hong‐Ping Xiao Ai‐Yin Wang Xin‐Hua Li Ali Morsali 《Helvetica chimica acta》2014,97(3):345-354
Two new silver(I) 3D coordination polymers, namely [Ag3(2‐stp)(dpa)]n ( 1 ) and {[Ag2(2‐stp)(H2O)]?Hdpa}n ( 2 ) (2‐NaH2stp=sodium 2,5‐dicarboxysulfonate, dpa=di(pyridine‐2‐yl)amine) were synthesized. The complexes were characterized by elemental analysis, FT‐IR spectra, thermogravimetric analyses (TGA), and single‐crystal X‐ray diffraction. In complex 1 , three neighboring Ag ions are bridged by N‐ and O‐atom, forming a 3D coordination network. The molecular structure of 2 is cation? anion species, forming 3D host? guest supramolecular network with the [Hdpa]+ cations encapsulated in the nanochannels. The photoluminescence properties of the complexes were also investigated in the solid state at room temperature. 相似文献
78.
Nanostructured -y-A12O3 with high surface area and mesoporous structure was synthesized by sol-gel method and employed as catalyst support for nickel catalysts in methane reforming with carbon dioxide. The prepared samples were characterized by XRD, N2 adsorption-desorption, TPR, TPO, TPH, NH3-TPD and SEM techniques. The BET analysis showed a high surface area of 204 m2.g-1 and a narrow pore-size distribution centered at a diameter of 5.5 nm for catalyst support. The BET results revealed that addition of lanthanum oxide to aluminum oxide decreased the specific surface area. In addition, TPR results showed that addition of lanthanum oxide increased the reducibility of nickel catalyst. The catalytic evaluation results showed an increase in methane conversion with increasing lanthanum oxide to 3 mol% and further increase in lanthanum content decreased the catalytic activity. TPO analysis revealed that the coke deposition decreased with increasing lanthanum oxide to 3 mol%. SEM and TPH analyses confirmed the formation of whisker type carbon over the spent catalysts. Addition of steam and Oxide to drv reformin feed increased the methane conversion and led to carbon free ooeration in combined orocesses. 相似文献
79.
Nanostructured γ-Al2O3 with high surface area and mesoporous structure was synthesized by sol-gel method and employed as catalyst support for nickel catalysts in methane reforming with carbon dioxide. The prepared samples were characterized by XRD, N2adsorption-desorption,TPR, TPO, TPH, NH3-TPD and SEM techniques. The BET analysis showed a high surface area of 204 m2 g-1and a narrow pore-size distribution centered at a diameter of 5.5 nm for catalyst support. The BET results revealed that addition of lanthanum oxide to aluminum oxide decreased the specific surface area. In addition, TPR results showed that addition of lanthanum oxide increased the reducibility of nickel catalyst. The catalytic evaluation results showed an increase in methane conversion with increasing lanthanum oxide to 3 mol% and further increase in lanthanum content decreased the catalytic activity. TPO analysis revealed that the coke deposition decreased with increasing lanthanum oxide to 3 mol%. SEM and TPH analyses confirmed the formation of whisker type carbon over the spent catalysts. Addition of steam and O2 to dry reforming feed increased the methane conversion and led to carbon free operation in combined processes. 相似文献
80.
New Polydentate Trimethylsilyl Chalcogenide Reagents for the Assembly of Polyferrocenyl Architectures 下载免费PDF全文
Mahmood Azizpoor Fard Bahareh Khalili Najafabadi Mahdi Hesari Prof. Dr. Mark S. Workentin Prof. Dr. John F. Corrigan 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(23):7037-7047
A series of polychalcogenotrimethylsilane complexes Ar(CH2ESiMe3)n, (Ar=aryl; E=S, Se; n=2, 3, and 4) can be prepared from the corresponding polyorganobromide and M[ESiMe3] (M=Na, Li). These represent the first examples of the incorporation of such a large number of reactive ?ESiMe3 moieties onto an organic molecular framework. They are shown to be convenient reagents for the preparation of the polyferrocenylseleno‐ and thioesters from ferrocenoyl chloride. The synthesis, structures, and spectroscopic properties of the new silyl chalcogen complexes 1,4‐(Me3SiECH2)2(C6Me4) (E=S, 1 ; E=Se, 2 ), 1,3,5‐(Me3SiECH2)3(C6Me3) (E=S, 3 ; E=Se, 4 ) and 1,2,4,5‐(Me3SiECH2)4(C6H2) (E=S, 5 ; E=Se, 6 ) and the polyferrocenyl chalcogenoesters [1,4‐{FcC(O)ECH2}2(C6Me4)] (E=S, 7 ; E=Se, 8 ), [1,3,5‐{FcC(O)ECH2}3(C6Me3)] (E=S, 9 ; E=Se, 10 ) and [1,2,4,5‐{FcC(O)ECH2}4(C6H2)] (E=S, 11 illustrated; E=Se, 12 ) are reported. The new polysilylated reagents and polyferrocenyl chalcogenoesters have been characterized by multinuclear NMR spectroscopy (1H, 13C, 77Se), electrospray ionization mass spectrometry and, for complexes 1 , 2 , 3 , 4 , 7 , 8 , and 11 , single‐crystal X‐ray diffraction. The cyclic voltammograms of complexes 7 – 11 are presented. 相似文献