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Surface modification of azide-decorated polyimide (PI) nanofibers with well-defined alkyne-terminated poly(methyl methacrylate) (PMMA) was accomplished via the combination of atom transfer radical polymerization (ATRP) and "click" chemistry. In this work, PI nanofibers were prepared via electrospun polyamic acid (PAA), followed by thermal imidization. Grafting of PMMA onto PI nanofibers was accomplished in three steps: (1) choloromethylation and azidization of PI nanofibers; (2) preparation of alkyne-terminated PMMA by ATRP of methyl methacrylate in toluene using propargyl 2-bromopropionate as initiator; (3) click coupling between the azidized PI nanofibers and the alkyne-terminated PMMA under the catalysis of Cu(I)Br/N,N,N',N''-pentamethyldiethylenetriamine (PMDETA). Gel permeation chromatography (GPC), (1)H NMR, and Fourier transform infrared (FT-IR) all confirmed the structure of alkyne-terminated poly(methyl methacrylate). The modified surface was characterized by X-ray photoelectron spectroscopy (XPS) after each modification stage. XPS and scanning electron microscope (SEM) were utilized to confirm PMMA-functionalized PI nanofibers, showing polymer coatings present on the surface of PI nanofibers. PI-g-PMMA nanofibers exhibited a more significant reinforcing effect compared to that with ungrafted PI nanofibers.
ACS Appl Mater Interfaces 2009 Dec
PMID:Grafting poly(methyl methacrylate) onto polyimide nanofibers via "click" reaction. 2035 60

Dialkyldithiophosphates (DTPs) of zinc(II), copper(II), and other metals have been extensively used as multifunctional additives in lubricants to control friction and reduce wear in mechanical systems. Among these DTP compounds, zinc dialkyldithiophosphates (ZnDTPs) are the most common additives extensively used for more than 60 years. These additives form a protective film on steel surfaces and, thus, control friction and reduce wear. However, ZnDTPs contain zinc and large amounts of phosphorus and sulfur, which impair the environment, both directly and indirectly, by adversely affecting the performance of catalytic converters of various automobiles. For this reason, environmental legislation imposes limitations on concentrations of phosphorus, sulfur, and zinc in the lubricants. In this work, we report on zinc-free S-di-n-octoxyboron-O,O'-di-n-octyldithiophosphate (DOB-DTP) lubricant additive with amount of phosphorus and sulfur reduced by half in a molecule as compared with ZnDTPs. DOB-DTP was synthesized by a reaction in two steps under inert nitrogen atmosphere. The final product, a viscous liquid, was characterized by the elemental analysis, FT-IR, multinuclear (1)H, (13)C, (31)P, and (11)B NMR spectroscopy and thermal analyses. Tribological performance of a mineral oil with this new additive was evaluated in comparison with O,O'-di-n-butyl-dithiophosphato-zinc(II) (ZnDTP) using a four-ball tribometer. The surface morphology and the elemental composition of the tribofilms were characterized using scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDS). The results show that DOB-DTP has a considerably better antiwear performance and higher stability of the coefficient of friction with time as compared with ZnDTP. Both phosphorus and sulfur were detected by the EDS on the worn steel surfaces at all concentrations of additives in the base oil.
ACS Appl Mater Interfaces 2009 Dec
PMID:Synthesis, physicochemical, and tribological characterization of S-Di-n-octoxyboron-O,O'-di-n-octyldithiophosphate. 2035 64

Polymer electrolytes based on mixtures of poly(ethylene oxide-co-propylene oxide) and 1-methyl-3-propyl-imidazolium iodide (MPII) were investigated, aiming at their application in dye-sensitized solar cells (DSSC). The interactions between the copolymer and the ionic liquid were analyzed by infrared spectroscopy and (1)H NMR. The results show interactions between the ether oxygen in the polymer and the hydrogen in the imidazolium cations. The ionic conductivities, electrochemical behaviors, and thermal properties of the electrolytes containing different concentrations of MPII were investigated. The electrolyte containing 70 wt % MPII presented the highest ionic conductivity (2.4 x 10(-3) S cm(-1)) and a diffusion coefficient of 1.9 x 10(-7) cm(2) s(-1). The influence of LiI addition to the electrolytes containing different concentrations of MPII was also investigated. The DSSC assembled with the electrolyte containing 70 wt % MPII showed an efficiency of 3.84% at 100 mW cm(-2). The stability of the devices for a period of 30 days was also evaluated using sealed cells. The devices assembled with the electrolyte containing less ionic liquid showed to be more stable.
ACS Appl Mater Interfaces 2009 Dec
PMID:Electrochemical and structural characterization of polymer gel electrolytes based on a PEO copolymer and an imidazolium-based ionic liquid for dye-sensitized solar cells. 2035 69

This paper reports a novel approach to designing advanced solid Li ion electrolytes for application in various solid state ionic devices, including Li ion secondary batteries, gas sensors, and electrochromic displays. The employed methodology involves a solid-solution reaction between the two best-known fast Li ion conductors in the garnet-family of compounds Li(6)BaLa(2)M(2)O(12) (M = Nb, Ta) and Li(7)La(3)Zr(2)O(12). Powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), AC impedance, and (7)Li nuclear magnetic resonance (Li NMR) spectroscopy were employed to characterize phase formation, morphology, ionic conductivity, and Li ion coordination in Li(6.5)La(2.5)BaZrMO(12). PXRD shows for formation of a cubic garnet-like structure and AC impedance data is consistent with other known solid Li ion electrolytes. Li(6.5)La(2.5)BaZrTaO(12) exhibits a fast Li ion conductivity of about 6 x 10(-3) S cm(-1) at 100 degrees C, which is comparable to that of currently employed organic polymer electrolytes value at room temperature. The Nb analogue shows an order of magnitude lower ionic conductivity than that of the corresponding Ta member, which is consistent with the trend in garnet-type electrolytes reported in the literature. Samples sintered at 1100 degrees C shows the highest electrical conductivity compared to that of 900 degrees C. (7)Li MAS NMR shows a sharp single peak at 0 ppm with respect to LiCl, which may be attributed to fast migration of ions between various sites in the garnets, and also suggesting average distributions of Li ions at average octahedral coordination in Li(6.5)La(2.5)BaZrMO(12). The present work together with literature used to establish very important fundamental relationship of functional property-Li concentration-crystal structure-Li diffusion coefficient in the garnet family of Li ion electrolytes.
ACS Appl Mater Interfaces 2010 Feb
PMID:Tailor-made development of fast Li ion conducting garnet-like solid electrolytes. 2035 83

Functionalized carbon nanotube (CNT) derivatives are currently under thorough investigation in different biomedical investigations. In this field of research, the composition of sample either in terms of covalently attached or physisorbed moieties can greatly affect the observed results and hamper the comparison between different studies. Therefore, the availability of a fast and reliable analytical technique to assess both the type of interaction (covalent vs noncovalent) and the composition of CNT conjugates is of great importance. Here we describe that the two-dimensional diffusion-ordered (DOSY) NMR spectroscopy is extremely useful to discriminate between conjugated and unconjugated polyethylene glycol groups in samples obtained by condensation with oxidized single-walled carbon nanotubes (SWNTs). This fast and nondestructive technique allows us to follow the removal of unconjugated polyethylene glycol chains during the purification. In particular, DOSY analysis reveal that about 1/3 (wt %) of the polyethylene glycol used for the condensation remained physisorbed to functionalized SWNTs after dialysis. Complete elimination of physisorbed polyethylene glycol was achieved using diafiltration.
ACS Nano 2010 Apr 27
PMID:Two-dimensional diffusion-ordered NMR spectroscopy as a tool for monitoring functionalized carbon nanotube purification and composition. 2035 36

A blend of phenyl-substituted, branched polysilane, (Ph(2)Si)(0.85)(PhSi)(0.15), and polystyrene (1:1 in weight) has been transformed into a composite material consisting of graphene layers, Si-O-C glasses, and micropores through a pyrolytic polymer-to-ceramic conversion. Several analytical techniques have been employed to characterize the Si-O-C composite material, demonstrating the presence of the three components in its host framework. The Si-O-C composite material performs well in electrochemical operations with a characteristic voltage plateau, offering a capacity of more than 600 mA h g(-1). When polystyrene is not blended, the resulting comparative material is even less porous and shows a shorter voltage plateau in electrochemical operations. A broad resonance in the (7)Li NMR spectrum recorded at low temperature can be deconvoluted into three components in the fully lithiated state of the Si-O-C composite material derived from the polymer blend. This result indicates that the Si-O-C composite material electrochemically stores lithium species in interstitial spaces or edges of the graphene layers, directly or indirectly the Si-O-C glass phase, and the micropores. However, both the Si-O-C glass phase and micropores are minor as electrochemically active sites for lithium storage, and interstitial spaces or edges of the graphene layers act as major electrochemically active sites in this composite material. Despite the excellent cyclability of the Si-O-C composite material, the voltage plateau disappeared over cycling. This phenomenon suggests that the microstructure is delicate for repetitive lithium insertion and extraction and that newly formed sites must generate the nearly equal capacity.
ACS Appl Mater Interfaces 2010 Apr
PMID:A Si-O-C composite anode: high capability and proposed mechanism of lithium storage associated with microstructural characteristics. 2042 19

Heat shock protein 70 (Hsp70) is a highly conserved molecular chaperone that plays multiple roles in protein homeostasis. In these various tasks, the activity of Hsp70 is shaped by interactions with co-chaperones, such as Hsp40. The Hsp40 family of co-chaperones binds to Hsp70 through a conserved J-domain, and these factors stimulate ATPase and protein-folding activity. Using chemical screens, we identified a compound, 115-7c, which acts as an artificial co-chaperone for Hsp70. Specifically, the activities of 115-7c mirrored those of a Hsp40; the compound stimulated the ATPase and protein-folding activities of a prokaryotic Hsp70 (DnaK) and partially compensated for a Hsp40 loss-of-function mutation in yeast. Consistent with these observations, NMR and mutagenesis studies indicate that the binding site for 115-7c is adjacent to a region on DnaK that is required for J-domain-mediated stimulation. Interestingly, we found that 115-7c and the Hsp40 do not compete for binding but act in concert. Using this information, we introduced additional steric bulk to 115-7c and converted it into an inhibitor. Thus, these chemical probes either promote or inhibit chaperone functions by regulating Hsp70-Hsp40 complex assembly at a native protein-protein interface. This unexpected mechanism may provide new avenues for exploring how chaperones and co-chaperones cooperate to shape protein homeostasis.
ACS Chem Biol 2010 Jun 18
PMID:Binding of a small molecule at a protein-protein interface regulates the chaperone activity of hsp70-hsp40. 2048 74

Kinetics and the atomic detail of RNA refolding are only poorly understood. It has been proposed that conformations with transient base pairing interaction are populated during RNA refolding, but a detailed description of those states is lacking. By NMR and CD spectroscopy, we examined the refolding of a bistable RNA and the influence of urea, Mg(2+), and spermidine on its refolding kinetics. The bistable RNA serves as a model system and exhibits two almost equally stable ground-state conformations. We designed a photolabile caged RNA to selectively stabilize one of the two ground-state conformations and trigger RNA refolding by in situ light irradiation in the NMR spectrometer. We can show that the refolding kinetics of the bistable RNA is modulated by urea, Mg(2+), and spermidine by different mechanisms. From a statistical analysis based on elementary rate constants, we deduce the required number of base pairs that need to be destabilized during the refolding transition and propose a model for the transition state of the folding reaction.
ACS Chem Biol 2010 Aug 20
PMID:Probing mechanism and transition state of RNA refolding. 2053 61

A new synthetically facile heteroleptic ruthenium(II) sensitizer (NBu(4))[Ru(4,7-dpp)(dcbpyH)(NCS)(2)], coded as YS5, where NBu(4) is tetrabutylammonium, 4,7-dpp is 4,7-diphenyl-1,10-phenanthroline, and dcbpyH is the singly deprotonated surface anchoring derivative of 4,4'-dicarboxy-2,2'-bipyridine (dcbpyH(2)), was designed, synthesized, and incorporated into regenerative mesoscopic titania-based dye-sensitized solar cells. The sensitizer has characteristic broad, high extinction coefficient MLCT bands spanning the visible spectrum. The compound was fully characterized by 1D and 2D (1)H NMR, MALDI-TOF-MS, UV-vis, photoluminescence, Raman, IR, and electrochemistry. YS5 exhibits strong visible absorption properties with a molar extinction coefficient of 1.71 x 10(4) M(-1) cm(-1) at its 522 nm maximum. In operational liquid junction-based DSSCs under simulated AM 1.5G one-sun excitation (100 mW/cm(2)), the photovoltaic performance of YS5 compares almost equally against the current benchmark sensitizer N719 in side-by-side comparisons, producing a power conversion efficiency of 6.05% with a maximum IPCE of 65% at 540 nm. The data presented in this manuscript strongly suggest that YS5 is indeed a viable sensitizer for nanocrystalline TiO(2)-based DSSCs, seemingly poised for widespread adaptation.
ACS Appl Mater Interfaces 2010 Jul
PMID:Viable alternative to N719 for dye-sensitized solar cells. 2056 60

Generally, antimicrobial N-halamine siloxane coatings can be rehalogenated repetitively upon loss of their biocidal efficacies, a marked advantage over coatings containing other antimicrobial materials. However, the N-halamine materials tend to slowly decompose upon exposure to ultraviolet irradiation as in direct sunlight. In this work the mechanism of photolytic decomposition for the N-halamine siloxanes has been studied using spectroscopic and theoretical methods. It was found that the N-chlorinated coatings slowly decomposed upon UVA irradiation, whereas the unhalogenated coatings did not. Model compound evidence in this work suggests that upon UVA irradiation, the N-Cl bond dissociates homolytically, followed by a Cl radical migration to the alkyl side chain connected to the siloxane tethering group. An alpha and/or beta scission then occurs causing partial loss of the biocidal moiety from the surface of the coated material, thus precluding complete rechlorination. NMR, FTIR, GCMS, and computations at the DFT (U)B3LYP/6-311++G(2d,p) level of theory have been employed in reaching this conclusion.
ACS Appl Mater Interfaces 2010 Aug
PMID:Mechanism of photolytic decomposition of N-halamine antimicrobial siloxane coatings. 2066 10


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