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101.
Bruno Morandi Pires Willian Goncalves Nunes Bruno Guilherme Freitas Francisca Elenice Rodrigues Oliveira Vera Katic Cristiane Barbieri Rodella Leonardo Morais Da Silva Hudson Zanin 《Journal of Energy Chemistry》2021,(3):53-62
We report here the activated carbon and cobalt hexacyanoferrate composite,which is applied as the electrode materials in symmetric supercapacitors containing a 1.0 M Na2SO4 aqueous electrolyte.This novel material combines high specific surface area and electrochemical stability of activated carbon with the redox properties of cobalt hexacyanoferrate,resulting in maximum specific capacitance of 329 F g-1 with large voltage working window of 2.0 V.Electrochemical studies indicated that cobalt hexacyanoferrate introduces important pseudocapacitive properties accounting for the overall charge-storage process,especially when I<0.5 A g-1.At lower gravimetric currents(e.g.,0.05 A g-1)and up to 1.0 V,the presence of cobalt hexacyanoferrate improves the specific energy for more than 300%.In addition,to better understanding the energy storage process we also provided a careful investigation of the electrode materials under dynamic polarization conditions using the in situ Raman spectroscopy and synchrotron light Xray diffraction techniques.Interesting complementary findings were obtained in these studies.We believe that this novel electrode material is promising for applications regarding the energy-storage process in pseudocapacitors with long lifespan properties. 相似文献
102.
Ignacio Alfonso Bernard Dietrich Francisca Rebolledo Vicente Gotor Jean‐Marie Lehn 《Helvetica chimica acta》2001,84(2):280-295
The protonation features of two optically active 22‐membered hexaazamacrocycles possessing one ( L1 ) or two ( L2 ) (R,R)‐cyclohexane‐1,2‐diamine moieties have been studied by means of potentiometric 1H‐ and 13C‐NMR techniques. This study allows the determination of the basicity constants and the stepwise protonation sites. The presence of the cyclohexane decreases the protonation ability, and this effect can be explained in terms of conformational and electrostatic factors. Binding of different chiral dicarboxylates has been studied by potentiometry. Macrocycle L2 presents higher anion‐complexation equilibrium constants than L1 . The stability of the diastereoisomeric complexes depends on the pH, and the structures of the macrocycles and anions. Receptor L1 ⋅6 H+ shows moderate D ‐selectivity towards tartrate anion, whereas L2 ⋅6 H+ exhibits a good preference for N‐Ac‐D ‐aspartate. Both protonated L1 and L2 form strong complexes with N‐Ac‐glutamate, and the stoichiometry of the complex depends on the degree of protonation and the absolute configuration of the anion. For this last anion, both azamacrocycles exhibit a clear D ‐preference. 相似文献
103.
Hiranthi Jayasuriya KithsiriB. Herath Chaowei Zhang DeborahL. Zink Angela Basilio Olga Genilloud MariaTeresa Diez Francisca Vicente Ignacio Gonzalez Oscar Salazar Fernando Pelaez Richard Cummings Sookhee Ha Jun Wang SheoB. Singh 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2007,119(25):4768-4772
104.
Anayive P. Rebolledo Geraldo M. de Lima Lillian N. Gambi Nivaldo L. Speziali Daniel F. Maia Carlos B. Pinheiro Jos D. Ardisson Maria Esperanza Corts Heloisa Beraldo 《应用有机金属化学》2003,17(12):945-951
Three tin(IV) complexes of 2‐benzoylpyridine N(4)‐phenylthiosemicarbazone (H2Bz4Ph) were prepared: [Sn(L)Cl3] (1), [BuSn(L)Cl2] (2) and [(Bu)2Sn(L)Cl] (3), in which L stands for the anionic ligand formed upon complexation with deprotonation and release of HCl. The complexes were characterized by a number of spectroscopic techniques. The crystal structures of H2Bz4Ph and complex 3 were determined. The antifungal activity of the ligand and its tin(IV) complexes was tested against Candida albicans. The thiosemicarbazone proved to be more active than the tin(IV) complexes. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
105.
Fernando J. S. Oliveira Leonardo Vazquez Norberto P. De Campos Francisca P. de Fran?a 《Applied biochemistry and biotechnology》1996,131(1-3):727-737
Biosurfactants production by a strain of Pseudomonas aeruginosa using palm oil as a sole carbon source was investigated. The experiments were carried out in 500-mL conical flasks containing
100 mL of mineral media supplemented with palm oil as the sole carbon source. The P. aeruginosa FR strain was able to reduce surface tension of three tested inorganic media. Rotation velocities from 100 to 150 rpm provided
free-cell fermented media with the lowest surface tension of approx 33 mN/m. Emulsification index results of even 100% were
achieved when diesel was used as oil phase. Eight surface-active compounds produced by the bacterium were identified by mass
spectrometry. 相似文献
106.
The synthesis and characterization of three heteronuclear Pt(2)Pd(2) (4, 5) and PtPd(2) (6) complexes of the model nucleobase 9-methyladenine (9-MeA) is reported. The compounds were prepared by reacting [Pt(NH(3))(3)(9-MeA-N7)](ClO(4))(2) (1) with [Pd(en)(H(2)O)(2)](ClO(4))(2) at different ratios r between Pt and Pd, with the goal to probe Pd(II) binding to any of the three available nitrogen atoms, N1, N3, N6 or combinations thereof. Pd(II) coordination occurs at N1 and at the deprotonated N6 positions, yet not at N3. 4 and 5 are isomers of [{(en)Pd}(2){N1,N6-9-MeA(-)-N7)Pt(NH(3))(3)}(2)](ClO(4))(6)·nH(2)O, with a head-head orientation of the two bridging 9-MeA(-) ligands in 4 and a head-tail orientation in 5. 6 is [{(en)Pd}(2)(OH)(N1,N6-9MeA(-)-N7)Pt(NH(3))(3)](ClO(4))(4)·4H(2)O, hence a condensation product between [Pt(NH(3))(3)(9-MeA-N7)](2+) and a μ-OH bridged dinuclear (en)Pd-OH-Pd(en) unit, which connects the N1 and N6 positions of 9-MeA(-) in an intramolecular fashion. 4 and 5, which slowly interconvert in aqueous solution, display distinct structural differences such as significantly different intramolecular Pd···Pd contacts (3.124 0(16) ? in 4; 2.986 6(14) ? in 5), among others. Binding of (en)Pd(II) to the exocyclic N6 atom in 4 and 5 is accompanied by a large movement of Pd(II) out of the 9-MeA(-) plane and a trend to a further shortening of the C6-N6 bond as compared to free 9-MeA. The packing patterns of 4 and 5 reveal substantial anion-π interactions. 相似文献
107.
Enzymatic catalysis has become a common tool in both academia and industrial chemistry. The efforts of chemists over recent decades have led to the rationalization of the mechanism of action of biocatalysts, which have been routinely incorporated into many synthetic sequences. Nowadays, a further step consists in expanding the application of enzymes to the modification of complex molecular scaffolds common to many pharmaceutical leads isolated from nature. Regioselective enzymatic acylation is a process which has been profitably applied for this purpose in recent times, leading to new drugs with improved activity, stability and pharmacokinetic properties. This tutorial review provides an overview of this subject employing two classes of enzymes, hydrolases and acyltransferases, in the recently concluded decade although some representative older studies are commented upon, if required. We shall place special emphasis on those examples in which the novel acylated derivatives have improved the activity or properties of the parental molecules. 相似文献
108.
A comparison between theoretical and experimental results of gain and ASE obtained with erbium-doped fibers (EDFs) pumped at 980 nm is presented. Parameters used for the calculations were deduced from a completely different experiment based on the study of fluorescence dynamics. The deduced parameters are not only the emission coefficents (equivalent to the emission cross-sections), but also the erbium concentration and its effective radial distribution. In the subsequent comparison of gain and amplified spontaneous emissions (ASE), a good agreement between theory and experiment is obtained. Therefore, combination of the usual theoretical model of EDFs and the characterization method that is proposed can give correct gain and ASE predictions. 相似文献
109.
Rodney Lacret Daniel Oves-Costales Ignacio Pérez-Victoria Mercedes de la Cruz Caridad Díaz Francisca Vicente 《Natural product research》2019,33(1):66-73
A new medermycin derivative, MDN-0171 (1), and two known structurally related compounds, medermycin (2) and antibiotic G15-F (3) were isolated from the acetone extract of culture broths of the marine-derived Streptomyces albolongus strain CA-186053. Their structures were determined using a combination of spectroscopic techniques, including 1D and 2D NMR and electrospray-time of flight mass spectrometry (ESI-TOF MS). Compounds 2 and 3 accounted for the antimicrobial activity (against methicillin-resistant Staphylococcus aureus and Escherichia coli) previously detected in the crude extract of this actinomycete. 相似文献
110.