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排序方式: 共有191条查询结果,搜索用时 218 毫秒
31.
TlI[(C4H9N4)PtII(CN)2] forms a red, crystalline polymorph in which the ions are arranged to form an extended ...Pt...Tl...Pt...Tl... chain (Pt...Tl distance, 3.0978(2) A; Pt-Tl-Pt and Tl-Pt-Tl angles, (171.37(2) degrees ) and a yellow polymorph in which dimers are connected by pairs of Pt...Tl interactions with a Pt...Tl distance of 3.0256(5) A. 相似文献
32.
Alan L. Balch Rosalvina R. Guimerans Marilyn M. Olmstead 《Journal of organometallic chemistry》1984,268(2):c38-c42
The preparation and interconversion of the following clusters bridged by bis(diphenylphosphinomethyl)phenylphosphine (dpmp) are reported: [Rh3(μ-dpmp)2(CO)aXb][BPh4]; X = I, a = 2, 3, 4, b = 2; X = I, a = 3, 2, 1, b = 4; X = I, a = 1, b = 6. The structure of one of these, [Rh3(μ-dpmp)2(CO)I4][BPh4], has been determined by X-ray diffraction. 相似文献
33.
Echegoyen L Chancellor CJ Cardona CM Elliott B Rivera J Olmstead MM Balch AL 《Chemical communications (Cambridge, England)》2006,(25):2653-2655
Crystallographic data for the pyrrolidine adduct Y3N@C80C4H9N x 2.5CS2 reveals a slightly pyramidalized Y3N unit with idealized mirror symmetry that straddles the site of addition but does not directly interact with the addend. 相似文献
34.
Nabil N. AL‐Hashimi Rand O. Shahin Aqeel N. AL‐Hashimi Ajeal M. Al Ajeal Lubna H. Tahtamouni Chanbasha Basheer 《Biomedical chromatography : BMC》2019,33(2)
A new cetyl‐alcohol‐reinforced hollow fiber solid/liquid‐phase microextraction (CA–HF–SLPME) followed by high‐performance liquid chromatography–diode array detection (HPLC–DAD) method was developed for simultaneous determination of ezetimibe and simvastatin in human plasma and urine samples. To prepare the CA–HF–SLPME device, the cetyl‐alcohol was immobilized into the pores of a 2.5 cm hollow fiber micro‐tube and the lumen of the micro‐tube was filled with 1‐octanol with the two ends sealed. Afterwards, the prepared device was introduced into 10 mL of the sample solution containing the analytes with agitation. Under optimized conditions, calibration curves plotted in spiked plasma and urine samples were linear in the ranges of 0.363–25/0.49–25 μg L?1 for ezetimibe/simvastatin and 0.193–25/0.312–25 μg L?1 for ezetimibe/simvastatin in plasma and urine samples, respectively. The limit of detection was 0.109/0.174 μg L?1 for ezetimibe/simvastatin in plasma and 0.058/0.093 μg L?1 for ezetimibe/simvastatin in urine. As a potential application, the proposed method was applied to determine the concentration of selected analytes in patient plasma and urine samples after medication and satisfactory results were achieved. In comparison with reference methods, the CA–HF–SLPME–HPLC–DAD method demonstrates considerable potential in the biopharmaceutical analysis of selected drugs. 相似文献
35.
Crystallographic and luminescence studies on salts of the two-coordinate carbene cation, [Au{C(NHCH(3))(NHCH(2)CH(2)OH)}(2)](+), demonstrate the ability of the cation to exist in three different states of aggregation. In colorless, non-luminescent [Au{C(NHCH(3))(NHCH(2)CH(2)OH)}(2)]Cl the cation crystallizes as a monomer with the nearest gold(i) center 6.7890(11) A away. Colorless, luminescent [Au{C(NHCH(3))(NHCH(2)CH(2)OH)}(2)]AsF(6) forms dimers with an AuAu separation of 3.1288(4) A. These dimers form weakly associated extended chains of cations with additional AuAu separations of 3.6625(5) A. [Au{C(NHCH(3))(NHCH(2)CH(2)OH)}(2)]PF(6) is isostructural. Yellow, luminescent [Au{C(NHCH(3))(NHCH(2)CH(2)OH)}(2)](3)(AsF(6))(2)Cl.0.5(H(2)O)(2) and [Au{C(NHCH(3))(NHCH(2)CH(2)OH)}(2)](3)(PF(6))(2)Cl.0.5(H(2)O)(2) form trimers that further aggregate into extended chains with rather short AuAu separations of 3.1301(14) A, 3.1569(14) A and 3.1415(14) A. Absorption, emission and excitation spectra are reported for these salts. The excitation and emission results from the interactions between the gold centers and involves transitions between the filled d(z)((2)) band and the empty p(z) bands with the z axis pointing along the chain of cations. 相似文献
36.
Synthesis and Isolation of the Titanium–Scandium Endohedral Fullerenes—Sc2TiC@Ih‐C80, Sc2TiC@D5h‐C80 and Sc2TiC2@Ih‐C80: Metal Size Tuning of the TiIV/TiIII Redox Potentials 下载免费PDF全文
Katrin Junghans Dr. Kamran B. Ghiassi Nataliya A. Samoylova Qingming Deng Marco Rosenkranz Prof. Marilyn M. Olmstead Prof. Alan L. Balch Dr. Alexey A. Popov 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(37):13098-13107
The formation of endohedral metallofullerenes (EMFs) in an electric arc is reported for the mixed‐metal Sc–Ti system utilizing methane as a reactive gas. Comparison of these results with those from the Sc/CH4 and Ti/CH4 systems as well as syntheses without methane revealed a strong mutual influence of all key components on the product distribution. Whereas a methane atmosphere alone suppresses the formation of empty cage fullerenes, the Ti/CH4 system forms mainly empty cage fullerenes. In contrast, the main fullerene products in the Sc/CH4 system are Sc4C2@C80 (the most abundant EMF from this synthesis), Sc3C2@C80, isomers of Sc2C2@C82, and the family Sc2C2 n (2 n=74, 76, 82, 86, 90, etc.), as well as Sc3CH@C80. The Sc–Ti/CH4 system produces the mixed‐metal Sc2TiC@C2 n (2 n=68, 78, 80) and Sc2TiC2@C2 n (2 n=80) clusterfullerene families. The molecular structures of the new, transition‐metal‐containing endohedral fullerenes, Sc2TiC@Ih‐C80, Sc2TiC@D5h‐C80, and Sc2TiC2@Ih‐C80, were characterized by NMR spectroscopy. The structure of Sc2TiC@Ih‐C80 was also determined by single‐crystal X‐ray diffraction, which demonstrated the presence of a short Ti=C double bond. Both Sc2TiC‐ and Sc2TiC2‐containing clusterfullerenes have Ti‐localized LUMOs. Encapsulation of the redox‐active Ti ion inside the fullerene cage enables analysis of the cluster–cage strain in the endohedral fullerenes through electrochemical measurements. 相似文献
37.
Chitosan loaded with silver nanoparticles,CS‐AgNPs,using thymus syriacus,wild mint,and rosemary essential oil extracts as reducing and capping agents 下载免费PDF全文
Fadi AL‐Shnani Thanaa Al‐Haddad Francois Karabet Abdul Wahab Allaf 《Journal of Physical Organic Chemistry》2017,30(11)
The present study describes the green method for the preparation of chitosan loaded with silver nanoparticles (CS‐AgNPs) in the presence of 3 different extracted essential oils. The essential oils play dual roles as reductant and capping agents. The reducing power and DPPH (2,2‐diphenyl‐1‐picrylhydrazyl) assay for the 3 essential oils—Thymus syriacus (T), wild mint (M), and rosemary (R)—have been reported. The preparation of CS‐AgNPs was performed by 2 steps. The 3 previously extracted essential oils have been used as reducing and capping agent in the first step, while in the second step, silver nanoparticles were integrated in chitosan. The integration of AgNPs in the structure of chitosan was confirmed by ultraviolet‐visible, Fourier transform infrared spectroscopy, scanning electron microscopy techniques, and energy dispersive X‐ray. Surface plasmon resonance confirmed the formation of CS‐AgNPs with maximum absorbance at λmax between 405 ‐ 410 and 410 ‐ 430 nm for colloidal and films of CS‐AgNPs, respectively. The intensity of bands at 3408 cm?1 in the fourier transform infrared spectroscopy measurements was decreased substantially and shifted slightly to lower frequency (?υ = 43 cm?1). Scanning electron microscopy shows a spherical morphology of AgNPs with size of 62 nm for both colloidal and film samples, and energy dispersive X‐ray analysis shows peaks confirming AgNPs formation. 相似文献
38.
Khaldun M. AL Azzam Bahruddin Saad Rohana Adnan Muhammad Idiris Saleh 《Mikrochimica acta》2009,166(3-4):311-317
A fast capillary electrophoretic method is described for the separation and determination of the enantiomers of the novel wake-promoting agent, modafinil. Several parameters affecting the separation were studied, including the type and concentration of chiral selector, buffer pH, buffer concentration, voltage and temperature. Good chiral separation of the racemic mixture was achieved in less than 5 min with resolution factor Rs?=?2.51, using a bare fused-silica capillary and a background electrolyte (BGE) of 25 mM H3PO4?1 M tris solution; pH 8.0; containing 30 mg mL?1 of sulfated-β-cyclodextrin (S-β-CD). The separation was carried out in normal polarity mode at 25 ?C, 18 kV and using hydrostatic injection. Acceptable validation criteria for selectivity, linearity, precision, and accuracy were included. The developed method was successfully applied to the assay of enantiomers of modafinil in pharmaceutical formulations. The computational calculations for the enantiomeric inclusion complexes rationalized the reasons for the different migration times between the modafinil enantiomers. 相似文献
39.
Reaction of Tl(I)NO(3) and (C(4)H(10)N(4))Pt(II)(mnt) or (C(4)H(10)N(4))Pt(II)(dmg-H) [mnt = maleonitriledithiolate, dmg-H = dimethylglyoximate dianion] in dilute, aqueous KOH yielded adducts of Tl(I) and the conjugate bases of the platinum(II) compounds. The compound Tl(I)[(C(4)H(9)N(4))Pt(II)(dmg-H)].5H(2)O forms as dimers with close Tl(I)...Pt(II) separations of 3.0843(5) A, while Tl(I)[(C(4)H(9)N(4))Pt(II)(mnt)] has much longer Tl(I)...Pt(II) separations of 3.4400(2) A and forms loosely associated, helical coordination polymers. The new compounds are compared with the red and yellow polymorphs of Tl(I)[(C(4)H(9)N(4))Pt(II)(CN)(2)], and the influences of crystal packing forces, Coulombic interactions, and hydrogen bonding on supramolecular structures and Tl(I)...Pt(II) separations are discussed. 相似文献
40.
Jin H Yang H Yu M Liu Z Beavers CM Olmstead MM Balch AL 《Journal of the American Chemical Society》2012,134(26):10933-10941
Two isomers of Sm@C(92) and four isomers of Sm@C(94) were isolated from carbon soot obtained by electric arc vaporization of carbon rods doped with Sm(2)O(3). Analysis of the structures by single-crystal X-ray diffraction on cocrystals formed with Ni(II)(octaethylporphyrin) reveals the identities of two of the Sm@C(92) isomers: Sm@C(92)(I), which is the more abundant isomer, is Sm@C(1)(42)-C(92), and Sm@C(92)(II) is Sm@C(s)(24)-C(92). The structure of the most abundant form of the four isomers of Sm@C(94), Sm@C(94)(I), is Sm@C(3v)(134)-C(94), which utilizes the same cage isomer as the previously known Ca@C(3v)(134)-C(94) and Tm@C(3v)(134)-C(94). All of the structurally characterized isomers obey the isolated pentagon rule. While the four Sm@C(90) and five isomers of Sm@C(84) belong to common isomerization maps that allow these isomers to be interconverted through Stone-Wales transformations, Sm@C(1)(42)-C(92) and Sm@C(s)(24)-C(92) are not related to each other by any set of Stone-Wales transformations. UV-vis-NIR spectroscopy and computational studies indicate that Sm@C(1)(42)-C(92) is more stable than Sm@C(s)(24)-C(92) but possesses a smaller HOMO-LUMO gap. While the electronic structures of these endohedrals can be formally described as Sm(2+)@C(2n)(2-), the net charge transferred to the cage is less than two due to some back-donation of electrons from π orbitals of the cage to the metal ion. 相似文献