聚二乙炴电子能带结构的研究

聚二乙炔(polydiacetylenes)具有平面的全共轭主链,并可被制备成宏观大小的单晶,因而是研究聚合物物理、化学性质的理想模型.它的物理、化学性质,特别是作为导电材料的导电机理与其价带及导带的结构密切相关.通过改变聚二乙炔的侧基可以对其主链几何结构及电子能带结构产生影响,进而改变其物理化学性质.可能是考     

Cyclic control of the surface properties of a monolayer-functionalized electrode by the electrochemical generation of Hg nanoclusters

Hg(2+) ions are bound to a 1,4-benzenedimethanethiol (BDMT) monolayer assembled on a Au electrode. Electrochemical reduction of the Hg(2+)-BDMT monolayer to Hg(+)-BDMT (at E degrees =0.48 V) and subsequently to Hg(0)-BDMT (at E degrees =0.2 V) proceeds with electron-transfer rate constants of 8 and 11 s(-1), respectively. The Hg(0) atoms cluster into aggregates that exhibit dimensions of 30 nm to 2 microm, within a time interval of minutes. Electrochemical oxidation of the nanoclusters to Hg(+) and further oxidation to Hg(2+) ions proceeds with electron-transfer rate constants corresponding to 9 and 43 s(-1), respectively, and the redistribution of Hg(2+) on the thiolated monolayer occurs within approximately 15 s. The reduction of the Hg(2+) ions to the Hg(0) nanoclusters and their reverse electrochemical oxidation proceed without the dissolution of mercury species to the electrolyte, implying high affinities of Hg(2+), Hg(+), and Hg(0) to the thiolated monolayer. The electrochemical transformation of the Hg(2+)-thiolated monolayer to the Hg(0)-nanocluster-functionalized monolayer is characterized by electrochemical means, surface plasmon resonance (SPR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), atomic force microscopy (AFM), and contact-angle measurements. The Hg(0)-nanocluster-modified surface reveals enhanced hydrophobicity (contact angle 76 degrees ) as compared to the Hg(2+)-thiolated monolayer (contact angle 57 degrees ). The hydrophobic properties of the Hg(0)-nanocluster-modified electrode are further supported by force measurements employing a hydrophobically modified AFM tip.     

Higher triplet excited states of benzophenones and bimolecular triplet energy transfer measured by using nanosecond-picosecond two-color/two-laser flash photolysis

The lifetimes of benzophenone in the higher triplet excited state (BP(T(n))) and several BP derivatives in the T(n) states were measured directly to be tau(T(n))=37+/-7 ps and 20-33 ps, respectively, by using the nanosecond-picosecond (ns-ps) two-color/two-laser flash photolysis method. Based on the direct measurements of tau(T(n)) of BP(T(n)), the triplet energy transfer (TET) from BP(T(n)) to quenchers (Q), such as carbon tetrachloride (CCl4), benzene (Bz), and p-dichlorbenzene (DCB), was investigated. The fast TET from BP(T(n)) to Q can be attributed to the lifetime-dependent quenching process, according to the Ware theoretical model of the bimolecular energy transfer reaction. The contribution of the lifetime-dependent term on k(TET) was 27, 60, and 86% for CCl4, Bz, and DCB as the Q of BP(T(n)), respectively, indicating that the TET from BP(T(n)) to Q is influenced not only by tau(T(n)), but also by the size of Q.     

Synthesis,structure, and reactivity of sp carbon chains with bis(phosphine) pentafluorophenylplatinum endgroups: butadiynediyl (C4) through hexadecaoctaynediyl (C16) bridges,and beyond

The reaction of trans-[(C(6)F(5))(p-tol(3)P)(2)PtCl] (PtCl) and butadiyne (cat. CuI, HNEt(2)) gives trans-[(C(6)F(5))(p-tol(3)P)(2)Pt(Ctbond;C)(2)H] (PtC(4)H, 81 %), which reacts with excess HC(triple bond)CSiEt(3) under Hay coupling conditions (O(2), cat. CuCl/TMEDA, acetone) to yield PtC(6)Si (53 %). A solution of PtC(6)Si in acetone is treated with wet nBu(4)NF to generate PtC(6)H. The addition of ClSiMe(3) (F(-) scavenger) and then excess HC(triple bond)CSiEt(3) under Hay conditions gives PtC(8)Si (39 %). Hay homocouplings of PtC(4)H, PtC(6)H, and PtC(8)H (generated in situ analogously to PtC(6)H) yield PtC(8)Pt, PtC(12)Pt, and PtC(16)Pt (97-92 %). Reactions of PtC(4)H and PtC(6)H with PtCl (cat. CuCl, HNEt(2)) give PtC(4)Pt and PtC(6)Pt (69 %, 34 %). The attempted conversion of PtC(8)H to PtC(10)Si affords mainly PtC(16)Pt, with traces of PtC(20)Pt and PtC(24)Pt. The complexes PtC(x)Pt are exceedingly stable (dec pts 234 to 288 degrees C), and Et(3)P displaces p-tol(3)P to give the corresponding compounds Pt'C(8)Pt' and Pt'C(12)Pt' (94-90 %). The effect of carbon chain lengths upon IR nu(C(triple bond)C) patterns (progressively more bands), UV/Vis spectra (progressively red-shifted and more intense bands with epsilon >600 000 M(-1) cm(-1)), redox properties (progressively more difficult and less reversible oxidations), and NMR values are studied, and analyzed with respect to the polymeric sp carbon allotrope "carbyne". The crystal structure of PtC(12)Pt shows a dramatic, unprecedented degree of chain bending, whereas the chains in PtC(8)Pt, Pt'C(12)Pt', and PtC(16)Pt are nearly linear.     

Heat-induced changes to lipid molecular structure in Vimy flaxseed: spectral intensity and molecular clustering

Autoclaving was used to manipulate nutrient utilization and availability. The objectives of this study were to characterize any changes of the functional groups mainly associated with lipid structure in flaxseed (Linum usitatissimum, cv. Vimy), that occurred on a molecular level during the treatment process using infrared Fourier transform molecular spectroscopy. The parameters included lipid CH(3) asymmetric (ca. 2959 cm(-1)), CH(2) asymmetric (ca. 2928 cm(-1)), CH(3) symmetric (ca. 2871 cm(-1)) and CH(2) symmetric (ca. 2954 cm(-1)) functional groups, lipid carbonyl CO ester group (ca. 1745 cm(-1)), lipid unsaturation group (CH attached to CC) (ca. 3010 cm(-1)) as well as their ratios. Hierarchical cluster analysis (CLA) and principal components analysis (PCA) were conducted to identify molecular spectral differences. Flaxseed samples were kept raw for the control or autoclaved in batches at 120°C for 20, 40 or 60 min for treatments 1, 2 and 3, respectively. Molecular spectral analysis of lipid functional group ratios showed a significant decrease (P<0.05) in the CH(2) asymmetric to CH(3) asymmetric stretching band peak intensity ratios for the flaxseed. There were linear and quadratic effects (P<0.05) of the treatment time from 0, 20, 40 and 60 min on the ratios of the CH(2) asymmetric to CH(3) asymmetric stretching vibration intensity. Autoclaving had no significant effect (P>0.05) on lipid carbonyl CO ester group and lipid unsaturation group (CH attached to CC) (with average spectral peak area intensities of 138.3 and 68.8 IR intensity units, respectively). Multivariate molecular spectral analyses, CLA and PCA, were unable to make distinctions between the different treatment original spectra at the CH(3) and CH(2) asymmetric and symmetric region (ca. 2988-2790 cm(-1)). The results indicated that autoclaving had an impact to the mid-infrared molecular spectrum of flaxseed to identify heat-induced changes in lipid conformation. A future study is needed to quantify the relationship between lipid molecular structure changes and functionality/availability.     

Structure and properties of the aluminum borates Al(BO2)n and Al(BO2)n(-), (n = 1-4)

The geometrical and electronic structures of Al(BO(2))(n) and Al(BO(2))(n)(-) (n = 1-4) clusters are computed at different levels of theory including density functional theory (DFT), hybrid DFT, double-hybrid DFT, and second-order perturbation theory. All aluminum borates are found to be quite stable toward the BO(2) and BO(2)(-) loss in the neutral and anion series, respectively. Al(BO(2))(4) belongs to the class of hyperhalogens composed of smaller superhalogens, and should possess a large adiabatic electron affinity (EA(ad)) larger than that of its superhalogen building block BO(2). Indeed, the aluminum tetraborate possesses the EA(ad) of 5.6 eV, which, however, is smaller than the EA(ad) of 7.8 eV of the AlF(4) supehalogen despite BO(2) is more electronegative than F. The EA(ad) decrease in Al(BO(2))(4) is due to the higher thermodynamic stability of Al(BO(2))(4) compared to that of AlF(4). Because of its high EA and thermodynamic stability, Al(BO(2))(4) should be capable of forming salts with electropositive counter ions. We optimized KAl(BO(2))(4) as corresponding to a unit cell of a hypothetical KAl(BO(2))(4) salt and found that specific energy and energy density of such a salt are competitive with those of trinitrotoluol (TNT).     

端基含甘露糖的聚赖氨酸的合成及其聚集行为

设计合成了2种含炔基的甘露糖衍生物(A-Man和A-DiMan)及2-[2-(2-叠氮乙氧基)-乙氧基]-乙胺(N3-TEG-NH2).以N3-TEG-NH2为引发剂引发Nε-苄氧羰基-L-赖氨酸酸酐(Lys(Z)-NCA)的开环聚合,得到2种分子量不同的端基含叠氮基团的聚赖氨酸,N3-P(Lys(Z))15和N3-P(Lys(Z))35,分别与A-Man和A-DiMan进行点击化学反应得到4种端基含甘露糖的聚合物.用透射电镜研究了4种聚合物在水溶液中的聚集行为,结果表明,基于P(Lys(Z))15的2种糖聚合物聚集形成囊泡,而基于P(Lys(Z))35的2种糖聚合物则聚集形成胶束.     

An ab initio/RRKM study of product branching ratios in the photodissociation of buta-1,2- and -1,3-dienes and but-2-yne at 193 nm

Ab initio G2M(MP2)//B3LYP/6-311G** calculations have been performed to investigate the reaction mechanism of photodissociation of buta-1,2- and -1,3-dienes and but-2-yne after their internal conversion into the vibrationally hot ground electronic state. The detailed study of the potential-energy surface was followed by microcanonical RRKM calculations of energy-dependent rate constants for individual reaction steps (at 193 nm photoexcitation and under collision-free conditions) and by solution of kinetic equations aimed at predicting the product branching ratios. For buta-1,2-diene, the major dissociation channels are found to be the single Cbond;C bond cleavage to form the methyl and propargyl radicals and loss of hydrogen atoms from various positions to produce the but-2-yn-1-yl (p1), buta-1,2-dien-4-yl (p2), and but-1-yn-3-yl (p3) isomers of C(4)H(5). The calculated branching ratio of the CH(3) + C(3)H(3)/C(4)H(5) + H products, 87.9:5.9, is in a good agreement with the recent experimental value of 96:4 (ref. 21) taking into account that a significant amount of the C(4)H(5) product undergoes secondary dissociation to C(4)H(4) + H. The isomerization of buta-1,2-diene to buta-1,3-diene or but-2-yne appears to be slower than its one-step decomposition and plays only a minor role. On the other hand, the buta-1,3-diene-->buta-1,2-diene, buta-1,3-diene-->but-2-yne, and buta-1,3-diene-->cyclobutene rearrangements are significant in the dissociation of buta-1,3-diene, which is shown to be a more complex process. The major reaction products are still CH(3) + C(3)H(3), formed after the isomerization of buta-1,3-diene to buta-1,2-diene, but the contribution of the other radical channels, C(4)H(5) + H and C(2)H(3) + C(2)H(3), as well as two molecular channels, C(2)H(2) + C(2)H(4) and C(4)H(4) + H(2), significantly increases. The overall calculated C(4)H(5) + H/CH(3) + C(3)H(3)/C(2)H(3) + C(2)H(3)/C(4)H(4) + H(2)/C(2)H(2) + C(2)H(4) branching ratio is 24.0:49.6:4.6:6.1:15.2, which agrees with the experimental value of 20:50:8:2:2022 within 5 % margins. For but-2-yne, the one-step decomposition pathways, which include mostly H atom loss to produce p1 and, to a minor extent, molecular hydrogen elimination to yield methylethynylcarbene, play an approximately even role with that of the channels that involve the isomerization of but-2-yne to buta-1,2- or -1,3-dienes. p1 + H are the most important reaction products, with a branching ratio of 56.6 %, followed by CH(3) + C(3)H(3) (23.8 %). The overall C(4)H(5) + H/CH(3) + C(3)H(3)/C(2)H(3) + C(2)H(3)/C(4)H(4) + H(2)/C(2)H(2) + C(2)H(4) branching ratio is predicted as 62.0:23.8:2.5:5.7:5.6. Contrary to buta-1,2- and -1,3-dienes, photodissociation of but-2-yne is expected to produce more hydrogen atoms than methyl radicals. The isomerization mechanisms between various isomers of the C(4)H(6) molecule including buta-1,2- and -1,3-dienes, but-2-yne, 1-methylcyclopropene, dimethylvinylidene, and cyclobutene have been also characterized in detail.     

Probing platinum azido complexes by 14N and 15N NMR spectroscopy

Metal azido complexes are of general interest due to their high energetic properties, and platinum azido complexes in particular because of their potential as photoactivatable anticancer prodrugs. However, azido ligands are difficult to probe by NMR spectroscopy due to the quadrupolar nature of (14)N and the lack of scalar (1)H coupling to enhance the sensitivity of the less abundant (15)N by using polarisation transfer. In this work, we report (14)N and (15)N NMR spectroscopic studies of cis,trans,cis-[Pt(N(3))(2)(OH)(2)(NH(3))] (1) and trans,trans,trans-[Pt(N(3))(2)(OH)(2)(X)(Y)], where X=Y=NH(3) (2); X=NH(3), Y=py (3) (py=pyridine); X=Y=py (4); and selected Pt(II) precursors. These studies provide the first (15)N NMR data for azido groups in coordination complexes. We discuss one- and three-bond J((15)N,(195)Pt) couplings for azido and am(m)ine ligands. The (14)N(α) (coordinated azido nitrogen) signal in the Pt(IV) azido complexes is extremely broad (W(1/2)≈2124 Hz for 4) in comparison to other metal azido complexes, attributable to a highly asymmetrical electric field gradient at the (14)N(α) atom. Through the use of anti-ringing pulse sequences, the (14)N NMR spectra, which show resolution of the broad (14)N(α) peak, were obtained rapidly (e.g., 1.5 h for 10 mM 4). The linewidths of the (14)N(α) signals correlate with the viscosity of the solvent. For (15) N-enriched samples, it is possible to detect azido (15)N resonances directly, which will allow photoreactions to be followed by 1D (15)N NMR spectroscopy. The T(1) relaxation times for 3 and 4 were in the range 5.7-120 s for (15)N, and 0.9-11.3 ms for (14)N. Analysis of the (1)J((15)N,(195)Pt) coupling constants suggests that an azido ligand has a moderately strong trans influence in octahedral Pt(IV) complexes, within the series 2-pic相似文献   

Torsional angular dependence of 1J(Se,Se) and Fermi contact control of 4J(Se,Se): analysis of nJ(Se,Se) (n=1-4) based on molecular orbital theory

(n)J(Se,Se) (n=1-4) nuclear couplings between Se atoms were analyzed by using molecular orbital (MO) theory as the first step to investigating the nature of bonded and nonbonded (n)J(Se,Se) interactions between Se atoms. The values were calculated by employing Slater-type triple xi basis sets at the DFT level, which were applied to structures optimized with the Gaussian 03 program. The contribution from each occupied MO (psi(i)) and psi(i)-->psi(a) (psi(a)=unoccupied MO) transition was evaluated separately. 1J(Se,Se) was calculated for the MeSeSeMe model compound, which showed a typical dependence on the torsion angle (phi(C(Me)SeSeC(Me))). This dependence explains the small values (< or =64 Hz) of 1Jobsd(Se,Se) observed for RSeSeR' and large values (330-380 Hz) of 1Jobsd(Se,Se) observed for 4-substituted naphtho[1,8-c,d]-1,2-diselenoles, which correspond to synperiplanar diselenides. The HOMO-->LUMO and HOMO-1-->LUMO transitions contribute the most to 1J(Se,Se) at phi=0 and 180 degrees to give large values of 1J(Se,Se), whereas various transitions contribute and cancel each other out at phi=90 degrees to give small values of 1J(Se,Se). Large 4Jobsd(Se,Se) values were also observed in the nonbonded Se...Se, Se...Se=O, and O=Se...Se=O interactions at naphthalene 1,8-positions. The Fermi contact (FC) term contributes significantly to 4J(Se,Se), whereas the paramagnetic spin-orbit (PSO) term contributes significantly to 1J(Se,Se). 2J(Se,Se) and 3J(Se,Se) were analyzed in a similar manner and a torsional angular dependence was confirmed for 3J(Se,Se). Depending on the structure, the main contribution to (n)J(Se,Se) (n=2, 3) is from the FC term, with a lesser contribution from the PSO term. Analysis of each transition enabled us to identify and clearly visualize the origin and mechanism of the couplings.     

Structural characterization of hexoses and pentoses using lead cationization. An electrospray ionization and tandem mass spectrometric study

The analytical potential of the complexation of isomeric underivatized hexoses (D-glucose, D-galactose, D-mannose, D-talose, D-fructose), methylglycosides (1-O-methyl-alpha-D-glucose and 1-O-methyl-beta-D-glucose) and pentoses (D-ribose, D-xylose, D-arabinose and D-lyxose) by Pb(2+) ions, was investigated by electrospray ionization and tandem mass spectrometry (MS/MS). Pb(2+) ions react mainly with monosaccharides by proton abstraction to generate [Pb(monosaccharide)(m) - H](+) ions (m = 1-3). At low cone voltage, a less abundant series of doubly charged ions of general formula [Pb(monosaccharide)(n)](2+) is also observed. The maximum number n of monosaccharides surrounding a single Pb(2+) ion depends on the metal : monosaccharide ratio. Our study shows that MS/MS experiments have to be performed to differentiate Pb(2+)-coordinated monosaccharides. Upon collision, [Pb(monosaccharide) - H](+) species mainly dissociate according to cross-ring cleavages, leading to the elimination of C(n)H(2n)O(n) neutrals. The various fragmentation processes observed allow the C(1), C(2) and C(4) stereocenters of aldohexoses to be characterized, and also a clear distinction aldoses and fructose. Furthermore, careful analysis of tandem mass spectra also leads to successful aldopentose distinction. Lead cationization combined with MS/MS therefore appears particularly useful to identify underivatized monosaccharides.     

N,N′-二乙(甲)基-N,N′-二苯基脲对铀(VI)和钍(IV)萃取行为的研究

目前国际上一般采用磷酸三丁酯(TBP)作为铀的萃取剂。TBP对铀有较强的萃取能力,但其耐辐照能力较差。酰胺的理化性质类似于TBP,与TBP相比降解产物易除去,“可完全燃烧”等优点而被认为是一种能取代应用于核燃料后处理的有前途的萃取剂。本文以二甲苯或三氯甲烷     

Silica-coated Ln3+-Doped LaF3 nanoparticles as robust down- and upconverting biolabels

The preparation of nearly monodisperse (40 nm), silica-coated LaF(3):Ln(3+) nanoparticles and their bioconjugation to FITC-avidin (FITC=fluorescein isothiocyanate) is described in this report. Doping of the LaF(3) core with selected luminescent Ln(3+) ions allows the particles to display a range of emission lines from the visible to the near-infrared region (lambda=450-1650 nm). First, the use of Tb(3+) and Eu(3+) ions resulted in green (lambda=541 nm) and red (lambda=591 and 612 nm) emissions, respectively, by energy downconversion processes. Second, the use of Nd(3+) gave emission lines at lambda=870, 1070 and 1350 nm and Er(3+) gave an emission line at lambda=1540 nm by energy downconversion processes. Additionally, the Er(3+) ions gave green and red emissions and Tm(3+) ions gave an emission at lambda=800 nm by upconversion processes when codoped with Yb(3+) (lambda(ex)=980 nm). Bioconjugation of avidin, which has a bound fluorophore (FITC) as the reporter, was carried out by means of surface modification of the silica particles with 3-aminopropyltrimethoxysilane, followed by reaction with the biotin-N-hydroxysuccinimide activated ester to form an amide bond, imparting biological activity to the particles. A 25-fold or better increase in the FITC signal relative to the non-biotinylated silica particles indicated that there is minimal nonspecific binding of FITC-avidin to the silica particles.     

Ferric and ferrous iron in nitroso-myoglobin: computer simulations of stable and metastable States and their infrared spectra.

The binding of NO to iron is involved in the biological function of many heme proteins. Contrary to ligands like CO and O(2), which only bind to ferrous (Fe(II)) iron, NO binds to both ferrous and ferric (Fe(III)) iron. In a particular protein, the natural oxidation state can therefore be expected to be tailored to the required function. Herein, we present an ab initio potential-energy surface for ferric iron interacting with NO. This potential-energy surface exhibits three minima corresponding to eta(1)-NO coordination (the global minimum), eta(1)-ON coordination and eta(2) coordination. This contrasts with the potential-energy surface for Fe(II)-NO, which exhibits only two minima (the eta(2) coordination mode for Fe(II) is a transition state, not a minimum). In addition, the binding energies of NO are substantially larger for Fe(III) than for Fe(II). We have performed molecular dynamics simulations for NO bound to ferric myoglobin (Mb(III)) and compare these with results obtained for Mb(II). Over the duration of our simulations (1.5 ns), all three binding modes are found to be stable at 200 K and transiently stable at 300 K, with eventual transformation to the eta(1)-NO global-minimum conformation. We discuss the implication of these results related to studies of rebinding processes in myoglobin.     

Stabilization of CoI by ZnII in pure acetonitrile and its reaction with aryl halides

The study of the electrochemical behavior of cobalt(II) bromide (CoBr(2)) in pure acetonitrile allowed us to demonstrate that Co(2+) is the catalyst precursor involved in the electrochemical and chemical conversions of arylhalides, ArX, to arylzinc compounds in that solvent. The reduction of Co(2+) leads to the Co(+) species, which disproportionates too rapidly to react further with aryl halides. However, the presence of zinc(II) bromide allows us to stabilize the electrogenerated cobalt(I) and to observe it on the timescale of slow cyclic voltammetry. Under such conditions, the Co(I) species has time to react with aryl halides and produce [Co(III)ArX](+) complexes that are reduced into [Co(II)ArX] by a single electron uptake at the same potential at which Co(2+) is reduced. Rate constants for the oxidative addition of ArX to Co(I) have been determined for various aryl halides and compared to the values obtained in an acetonitrile (ACN)/pyridine (9:1, v/v) mixture. It is shown that Co(I) is stabilized more by ZnBr(2) than by pyridine. A transmetallation reaction between [Co(II)ArX] and ZnBr(2) has also been observed. We finally propose a mechanism for the cobalt-catalyzed electrochemical conversion of aryl bromides into organozinc species in pure acetonitrile.     

Self-assembly of short peptide amphiphiles: the cooperative effect of hydrophobic interaction and hydrogen bonding

The interplay between hydrogen bonding, hydrophobic interaction and the molecular geometry of amino acid side-chains is crucial to the development of nanostructures of short peptide amphiphiles. An important step towards developing their practical use is to understand how different amino acid side-chains tune hydrophobic interaction and hydrogen bonding and how this process leads to the control of the size and shape of the nanostructures. In this study, we have designed and synthesized three sets of short amphiphilic peptides (I(3)K, LI(2)K and L(3)K; L(3)K, L(4)K and L(5)K; I(3)K, I(4)K and I(5)K) and investigated how I and L affected their self-assembly in aqueous solution. The results have demonstrated a strong tendency of I groups to promote the growth of β-sheet hydrogen bonding and the subsequent formation of nanofibrillar shapes. All I(m)K (m = 3-5) peptides assembled into nanofibers with consistent β-sheet conformation, whereas the nanofiber diameters decreased as m increased due to geometrical constraint in peptide chain packing. In contrast, L groups had a weak tendency to promote β-sheet structuring and their hydrophobicity became dominant and resulted in globular micelles in L(3)K assembly. However, increase in the number of hydrophobic sequences to L(5)K induced β-sheet conformation due to the cooperative hydrophobic effect and the consequent formation of long nanofibers. The assembly of L(4)K was, therefore, intermediate between L(3)K and L(5)K, similar to the case of LI(2)K within the set of L(3)K, LI(2)K and I(3)K, with a steady transition from the dominance of hydrophobic interaction to hydrogen bonding. Thus, changes in hydrophobic length and swapping of L and I can alter the size and shape of the self-assembled nanostructures from these simple peptide amphiphiles.     

Study of stereospecificity of 1H, 13C, 15N and 77Se shielding constants in the configurational isomers of the selenophene-2-carbaldehyde azine by NMR spectroscopy and MP2-GIAO calculations

In the (1)H and (13)C NMR spectra of selenophene-2-carbaldehyde azine, the (1)H-5, (13)C-3 and (13)C-5 signals of the selenophene ring are shifted to higher frequencies, whereas those of the (1)H-1, (13)C-1, (13)C-2 and (13)C-4 are shifted to lower frequencies on going from the EE to ZZ isomer or from the E moiety to the Z moiety of EZ isomer. The (15)N chemical shift is significantly larger in the EE isomer relative to the ZZ isomer and in the E moiety relative to the Z moiety of EZ isomer. A very pronounced difference (60-65 mg/g) between the (77)Se resonance positions is revealed in the studied azine isomers, the (77)Se peak being shifted to higher frequencies in the ZZ isomer and in the Z moiety of EZ isomer. The trends in the changes of the measured chemical shifts are reasonably reproduced by the GIAO calculations at the MP2 level of the (1)H, (13)C, (15)N and (77)Se shielding constants in the energy-favorable conformation with the syn orientation of both selenophene rings relative to the C = N groups. The NBO analysis suggests that such an arrangement of the selenophene rings may take place because of a higher energy of some intramolecular interactions.     

Synthesis of 9- and 27-armed tetrakis(diperoxotungsto)phosphate-cored dendrimers and their use as recoverable and reusable catalysts in the oxidation of alkenes, sulfides, and alcohols with hydrogen Peroxide

A series of 3- and 9-armed dendrons, functionalized at the focal position to quaternary ammonium salts, were synthesized and characterized. The reaction of these ammonium dendrons with the heteropolyacid H(3)PW(12)O(40) in the presence of hydrogen peroxide led to a family of 9- and 27-armed air-stable polyoxometalate (POM)-cored dendrimers containing a catalytically active trianionic POM species [PO(4)[WO(O(2))(2)](4)](3-) in the core. These POM-cored dendrimers are air-stable, efficient, recoverable, and reusable catalysts for the selective oxidation of alkenes to epoxides, sulfides to sulfones, and alcohols to ketones, in an aqueous/CDCl(3) biphasic system with hydrogen peroxide as the primary oxidant. A study of the countercation effects showed that the dendritic structure increased the stability of the POM species and facilitated the recovery of the catalyst up to the eighth cycle, whereas the increased bulkiness around the POM center led to a negative kinetic dendritic effect. Within the 9-armed POM-cored dendrimer series, the reaction kinetics were susceptible to the nature of the peripheral endgroups. Indeed, the 9-armed n-propyl-terminated POM-cored dendrimer was identified as the most active catalyst. In addition, the results obtained with POM-cored dendrimers versus tetraalkylammonium POMs ([[n-(C(8)H(17))(3)NCH(3)](+)](3)[PO(4)[WO(O(2))(2)](4)](3-) and [[nC(18)H(37)(75 %) + nC(16)H(33)(25 %)](2)N(CH(3))(2)](+)](3)[PO(4)[WO(O(2))(2)](4)](3-)) clearly reveal that the dendritic structures are more stable than their nondendritic counterparts. After the reactions were complete, the dendrimer catalysts were easily recovered and recycled without a discernable lost of activity, whereas attempts to recover tetraalkylammonium POMs gave unsatisfactory results. A significant advantage of the dendritic structures is that they enable the recovery and recyclability of the POM catalyst, in contrast to the other tetraalkylammonium POMs.     

甲基丙烯醛氧化酯化制甲基丙烯酸甲酯催化剂的制备与应用

甲基丙烯醛氧化酯化制甲基丙烯酸甲酯催化剂的制备与应用;催化剂; 甲基丙烯酸甲酯; 甲基丙烯醛; 氧化-酯化反应     

Isolation of rhenium and ReOx species within ZSM5 channels and their catalytic function in the activation of alkanes and alkanols

Synthesis protocols, structures, and reactivity of Re-oxo species grafted onto H-ZSM5, and their subsequent conversion to Re-clusters through contact with H2 or CH4 were studied by using Raman, infrared, and X-ray absorption spectroscopies. Reactivity measurements by using alkane and alkanol reactants were also examined. Sublimation of Re(2)O(7) at 723 K led to a stoichiometric exchange with each ReO(x) species replacing one proton. Raman features for Re(2)O(7) disappeared during thermal treatment and Raman bands assigned to distorted-tetrahedral Si-O(f)ReO(3)-Al (O(f): zeolite-lattice oxygen atoms) species emerged; infrared bands for acidic OH groups in H-ZSM5 weakened concurrently. X-ray absorption near-edge and fine-structure spectra detected the formation of distorted-tetrahedral Re7+-oxo species during thermal treatment of Re(2)O(7)/H-ZSM5 mixtures in air, and their subsequent reduction to Re(0) in H2 or CH4 to form encapsulated Re metal clusters similar in diameter (approximately 8 A) to the channel intersections in ZSM5. Si-O(f)ReO(3)-Al species in ReO(x)-ZSM5 catalyzed the oxidative conversion of C(2)H(5)OH to acetaldehyde, acetal, and ethyl acetate with very low selectivity to CO(x) (<1 %). Unprecedented turnover rates were exhibited at temperatures much lower than previously found for ReO(x)-based catalysts, and without deactivation or sublimation processes ubiquitous in crystalline Re7+ compounds at temperatures required for catalysis. Encapsulated Re metal clusters formed by the reduction of Si-O(f)ReO(3)-Al precursors led to CH4 pyrolysis and C(3)H(8) dehydrocyclodimerization rates (per Re) that are higher than those previously reported for zeolite-based catalysts. The rate of CH4 conversion to benzene, by using Re-ZSM5, was approximately 30 % higher than that of the best reported catalysts, based on encapsulated MoC(x) clusters, whereas C(2)H(4) and C6+ arene selectivities were similar. C(3)H(8) activity and selectivity of Re-ZSM5 was significantly higher than that of Ga-ZSM5, the best reported catalyst for these reactions. Reaction rates (per Re) were independent of the Re/Al(f) (Al(f): aluminum framework) ratio for both Re and ReO(x) species. This is consistent with the uniform character of the structures formed during grafting of the ReO(x) species through sublimation and their ability to retain their homogeneity even after their reduction to encapsulated Re-clusters.