Group 4 phosphides, which are typically prepared at high temperatures (> 800 degrees C) over several days, are synthesized in self-propagating metathesis (exchange) reactions in seconds. These reactions produce cubic forms of zirconium phosphide (ZrP) and hafnium phosphide (HfP) which are normally made at temperatures greater than 1425 degrees C and 1600 degrees C, respectively. To test whether the high temperatures reached in the metathesis reactions are responsible for the formation of the cubic phases, inert salts are added to lower the maximum reaction temperatures. The lower temperature reactions still result in cubic phosphides, although smaller crystallites form. Further experiments with phosphorus addition indicate that the phosphorus content is not responsible for cubic phase formation. Templating is ruled out using lattice mismatched KCl and hexagonal ZnS as additives. Therefore, the direct synthesis of the high-temperature cubic phase in metathesis reactions appears to be caused by nucleation of the metastable cubic form that is then trapped by rapid cooling. Heating the cubic phase of either ZrP or HfP to 1000 degrees C for 18 h, or carrying out metathesis reactions in sealed ampules at 1000 degrees C, results only in the hexagonal phase. 相似文献
Cluster ions from fast atom bombardment of liquid alcohols and nitriles were examined using a continuous-flow technique. Protonated molecular MnH+ species are the dominant cluster ions observed in molecules of formula M. The abundances of the MnH+ cluster ions decrease monotonically with increasing n, and within a homologous series the MnH+ abundance diminishes more rapidly for higher molecular mass compounds. Reaction products (ROH)n(H2O)H+ and (ROH)n(ROR)H+ are observed also in the case of alcohols, and the ion abundances decrease with increasing n. Radiation damage yields fragment ions and ionic alkyl reaction products which are captured in solvent clusters. Semi-empirical molecular orbital methods were used to examine the energetics of cluster ion formation and decomposition pathways. Metastable decomposition processes exhibit only evaporative loss of monomers, with the probability of loss increasing sharply with n. The evaporative ensemble model of Klots was used to predict the cluster size-dependent trends of metastable dissociation processes observed for alcohol and nitrile cluster ions. 相似文献
Cellulose isolated from celery collenchyma is typical of the low-crystallinity celluloses that can be isolated from primary
cell-walls of higher plants, except that it is oriented with high uniformity. The diameter of the microfibrils of celery collenchyma
cellulose was estimated by three separate approaches: 13C NMR measurement of the ratio of surface to interior chains; estimation of the dimensions of the crystalline lattice from
wide angle X-ray scattering (WAXS) measurements using the Scherrer equation; and the observation that microfibrils of this
form of cellulose have the unusual property of packing into an irregular array from which small angle X-ray scattering (SAXS)
shows features of both form and interference functions. The interference function contributing to the SAXS pattern implied
a mean microfibril centre-to-centre distance of 3.6 nm, providing an upper limit for the diameter. However modelling of the
scattering pattern from an irregular array of microfibrils showed that the observed scattering curve could be matched at a
range of diameters down to 2.4 nm, with the intervening space more or less sparsely occupied by hemicellulose chains. The
lateral extent of the crystalline lattice normal to the 200 plane was estimated as a minimum of 2.4 nm by WAXS through the
Scherrer equation, and a diameter of 2.6 nm was implied by the surface: volume ratio determined by 13C NMR. The WAXS and NMR measurements both depended on the assumption that the surface chains were positioned within an extension
of the crystalline lattice. The reliability of this assumption is uncertain. If the surface chains deviated from the lattice,
both the WAXS and the NMR data would imply larger microfibril diameters within the range consistent with the SAXS pattern.
The evidence presented is therefore all consistent with microfibril diameters from about 2.4 to 3.6 nm, larger than has previously
been suggested for primary-wall cellulose. Some degree of aggregation may have occurred during the isolation of the cellulose,
but the larger microfibril diameters within the range proposed are a consequence of the novel interpretation of the experimental
data from WAXS and NMR and are consistent with previously published data if these are similarly interpreted. 相似文献
Celery collenchyma cell walls are typical of primary plant cell walls in their composition but contain unusually well-oriented
cellulose microfibrils that are packed with more regularity than normal, permitting small-angle X-ray scattering (SAXS) experiments
that would not otherwise be possible. Small-angle scattering data were obtained for the cell walls in essentially their native
state and for isolated cellulose, in a fibrous form that retained the physical shape and microfibril orientation of the native
cell walls. The scattering patterns showed a distinct peak attributed to the interference contribution to the convolution
of form and interference functions. The position of the peak attributed to the interference function implied a mean centre-to-centre
microfibril spacing of approximately 3.2 nm in dry isolated cellulose and 3.8 nm in dry cell walls. Hydration increased the
mean microfibril spacing in the cell walls to 5.4 nm but had only a small effect on the mean microfibril spacing of isolated
cellulose. In the scattering profile from intact, hydrated cell walls it was just possible to discern the position of the
first Bessel minimum, from which a microfibril diameter in the range 3.1–3.6 nm may be estimated. This estimate is likely
to include attached hemicellulose chains. Porod plots of scattering intensity indicated a relatively sharp interface between
microfibrils and their immediate surroundings. The SAXS data imply that cellulose microfibrils 2.6–3.0 nm in diameter are
not quite in lateral contact with one another in the isolated cellulose and are augmented by hemicelluloses and separated
by readily hydrated matrix polysaccharides in the native plant cell wall. 相似文献
We investigated the capability of an ordered array of microspheres to act as a template for deposition and ordering of a subsequent layer of microspheres. An evaporation-based technique was used to deposit monolayers of large colloidal spheres. A novel technique for selective deposition of polyelectrolyte film was used to stabilize the arrays and optimize the bead-substrate interaction. The template behavior of face-centered cubic and body-centered cubic (bcc) microsphere arrays was studied by optical and scanning electron microscopy, and the packing geometry was found to have a dramatic effect on the arrangement of the subsequent layer. A geometrical interpretation of the experimental data explains why a bcc bead array is well suited to act as a template for an additional layer of microspheres. 相似文献
Positive and negative cluster ions in methanol have been examined using a direct fast atom bombardment (FAB) probe technique. Positive ion (CH3OH)IIH + clusters with n = 1-28 have been observed and their clusters are the dominant ions in the low-mass region. Cluster-ion reaction products (CH3OH)II(H2O)H+ and (CH3OH)II(CH3OCH3)H+ are observed for a wide range of n and the abundances of these ions decrease with increasing n. The negative ion (CH3OH)II(CH3O)? clusters are also readily observed with n = 0-24 and these form the most-abundant negative ion series at low n. The (CH3OH)II(CH2O)?, (CH3OH)II(HIIO)(CH2O)? and (CH3OH)II(H2OXCH3O)? cluster ions are formed and the abundances of these ions approach those of the (CH3OH)II(CH3O)? ion series at high n. Cluster-ion structures and energetics have been examined using semi-empirical molecular orbital methods. 相似文献
Lipooligosaccharides (LOS) are major microbial virulence factors displayed on the outer membrane of rough-type Gram-negative bacteria. These amphipathic glycolipids are comprised of two domains, a core oligosaccharide linked to a lipid A moiety. Isolated LOS samples are generally heterogeneous mixtures of glycoforms, with structural variability in both domains. Traditionally, the oligosaccharide and lipid A components of LOS have been analyzed separately following mild acid hydrolysis, although important acid-labile moieties can be cleaved. Recently, an improved method was introduced for analysis of intact LOS by MALDI-TOF MS using a thin layer matrix composed of 2,4,6-trihydroxyacetophenone (THAP) and nitrocellulose. In addition to molecular ions, the spectra show in-source “prompt” fragments arising from regiospecific cleavage between the lipid A and oligosaccharide domains. Here, we demonstrate the use of traveling wave ion mobility spectrometry (TWIMS) for IMS-MS and IMS-MS/MS analyses of intact LOS from Neisseria spp. ionized by MALDI. Using IMS, the singly charged prompt fragments for the oligosaccharide and lipid A domains of LOS were readily separated into resolved ion plumes, permitting the extraction of specific subspectra, which led to increased confidence in assigning compositions and improved detection of less abundant ions. Moreover, IMS separation of precursor ions prior to collision-induced dissociation (CID) generated time-aligned, clean MS/MS spectra devoid of fragments from interfering species. Incorporating IMS into the profiling of intact LOS by MALDI-TOF MS exploits the unique domain structure of the molecule and offers a new means of extracting more detailed information from the analysis.
Iodine(III) reagents are used in catalytic one‐pot reactions, first as both oxidants and substrates, then as cross‐coupling partners, to afford chiral polyfunctionalized amines. The strategy relies on an initial catalytic auto C(sp3)?H amination of the iodine(III) oxidant, which delivers an amine‐derived iodine(I) product that is subsequently used in palladium‐catalyzed cross‐couplings to afford a variety of useful building blocks with high yields and excellent stereoselectivities. This study demonstrates the concept of self‐amination of the hypervalent iodine reagents, which increases the value of the aryl moiety. 相似文献
Based on reversed-phase high-performance liquid chromatography (RP-HPLC) and atmospheric pressure chemical ionization (APCI) mass spectrometry, a HPLC-MS method was developed to permit the rapid qualitative and quantitative analysis of azadirachtin and related tetranortriterpenoids from seeds and tissue cultures of Neem (Azadirachta indica). APCI+ standard scanning mass spectra of the major Neem triterpenoids were recorded and utilized to select suitable ions for selected ion monitoring (SIM). Transitions for selective reaction monitoring (SRM) were based on MS-MS experiments. Using SIM, major Neem triterpenoids were detected in callus culture material and seed kernels of A. indica. The limit of detection for azadirachtin in extract samples (approximately 1 ng ml(-1) or 10 pg in SIM mode) was determined to be (with respect to injected absolute amounts) approximately 1000-times lower than values quoted in the literature for existing HPLC methods (approximately 200 ng ml(-1) or 10 ng). In addition to high sensitivity, the HPLC-MS method is able to tolerate minimal sample preparation and purification, dramatically reducing total analysis time. 相似文献