Mannich-type reactions in the gas-phase: the addition of enol silanes to cyclic N-acyliminium ions

The intrinsic gas-phase reactivity of cyclic N-acyliminium ions in Mannich-type reactions with the parent enol silane, vinyloxytrimethylsilane, has been investigated by double- and triple-stage pentaquadrupole mass spectrometric experiments. Remarkably distinct reactivities are observed for cyclic N-acyliminium ions bearing either endocyclic or exocyclic carbonyl groups. NH-Acyliminium ions with endocyclic carbonyl groups locked in s-trans forms participate in a novel tandem N-acyliminium ion reaction: the nascent adduct formed by simple addition is unstable and rearranges by intramolecular trimethylsilyl cation shift to the ring nitrogen, and an acetaldehyde enol molecule is eliminated. An NSi(CH(3))(3)-acyliminium ion is formed, and this intermediate ion reacts with a second molecule of vinyloxytrimethylsilane by simple addition to form a stable acyclic adduct. N-Acyl and N,N-diacyliminium ions with endocyclic carbonyl groups, for which the s-cis conformation is favored, react distinctively by mono polar [4(+) + 2] cycloaddition yielding stable, ressonance-stabilized cycloadducts. Product ions were isolated via mass-selection and structurally characterized by triple-stage mass spectrometric experiments. B3LYP/6-311G(d,p) calculations corroborate the proposed reaction mechanisms.     

Selective cleavage of N-benzyl-protected secondary amines by triphosgene

A series of competition experiments has revealed that selective cleavage of N-benzyl-protected secondary amines can be achieved with triphosgene, thereby providing a useful range of carbamoyl chlorides.     

Extended closure model for Kaimal''s isopleths

Summary A closure model for the spectral equation of turbulent kinetic energy, in the case of a steady-state and horizontally homogeneous flow in a stably stratified surface boundary layer is developed by use of systematic dimensional analysis. All resulting arbitrary functions that describe transfer mechanisms are subsequently Taylor-expanded in terms of their (small) arguments. This procedure leads to the closure of the system in terms of arbitrary constants which can subsequently be determined by fitting of observational data. The resulting solution is tested through comparison with experimental curves drawn from the Kansas experiment and with a formerly developed model.     

Equilibrium and stability of off-axis periodically focused particle beams

A general equation for the centroid motion of free, continuous, intense beams propagating off axis in solenoidal periodic focusing fields is derived. The centroid equation is found to be independent of the specific beam distribution and may exhibit unstable solutions. A new Vlasov equilibrium for off-axis beam propagation is also obtained. The properties of the equilibrium and the relevance of centroid motion to beam confinement are discussed.     

Ultrastructural aspects of the mandibular gland of Melipona bicolor Lepeletier, 1836 (Hymenoptera: Apidae, Meliponi) in the castes

The mandibular gland in Melipona bicolor workers and queens was studied by scanning and transmission electron microscopy. There is no difference in the gland anatomy between the castes, but the transmission electron microscopy showed variation of the cellular ultrastructure according to the secretory phase of the gland in both castes. Smooth endoplasmic reticulum was abundant in the secretory cells of physogastric queens, indicating that these cells produce lipid secretion that is stored in granules with multi-lamellar bodies. Mitochondrial variations during the cell secretory cycle indicates their participation in the lipid synthesis. After secretion, release in the reservoir lumen through the collecting canals, the secretory cells contain many myelinic bodies, indicative of cellular regression.     

The ad hoc return channel: a low-cost solution for Brazilian interactive digital TV

The upcoming terrestrial digital television technology brings a new class of services to traditional TV sets. A set-top box may, for example, access the Internet and send email. The interactive return channel makes these new services possible. This channel allows TV viewers to interact by sending data back to the TV broadcaster. In this article we analyze the viability of a wireless ad hoc network to implement the return channel. For this purpose, an ad hoc network is a low-cost and flexible solution. We evaluate the performance of an ad hoc return channel using the IEEE 802.11 wireless technology for different Brazilian geographical scenarios. The results show that ad hoc networking is a promising solution for the return channel of Brazilian interactive digital TV     

SDN-based teleprotection and control power systems: A study of available controllers and their suitability

With the popularization of the smart grid paradigm, substation automation technology has gradually been upgraded with additional processing and communication capabilities within control and protection devices. Hence, the research community is pressured to find new, efficient, and reliable communication solutions for such a scenario. That task is complicated by the stringent temporal requirements defined by the International Electrotechnical Commission (IEC) 61850 standard for power system communication comprising teleprotection schemes. Further compounding the issue is the critical nature of the power grid, in which availability is definitely a strong requirement. Software-defined networking (SDN) may provide powerful tools to fulfill those requirements at acceptable costs. As such, this paper surveys and compares several available SDN controllers and their applicability to the teleprotection scenario. It further evaluates controllers in terms of capacity and resilience through experiments in an emulated environment.     

Reduction of oxide ions of uranium in single-filament surface-ionization mass spectrometry with application to rock samples

Ion-emission characteristics of a single-filament surface-ionization source for uranium are described. It is shown that a graphite coating over uranium samples enhances reduction of oxides to U⁺ and improves quantitative performance. Results obtained for uranium in several rock samples are in reasonable agreement with results reported by others.     

Quantitation of isomeric ethyl pyridine mixtures by multivariate calibration applied to ion-molecule reaction/collision-induced dissociation triple-stage mass spectra

In reactions of the distonic ion ⁺CH₂OCH₂ with the three isomeric ethyl pyridines, ionized methylene transfer occurs readily yielding distonic N-methylene-ethylpyridinium ions. On-line mass selection and 10 eV collision-induced dissociation (CID) of the CH₂⁺ transfer products yields characteristic fragment ions, which are formed via processes greatly influenced by the ortho, meta or para location of the ethyl substituent in the pyridine ring. Quantitation of mixtures of isomeric 2-, 3-, and 4-ethyl pyridines of varying compositions was then performed by multivariate calibration in the form of the partial least square (PLS) model applied to both single-stage (MS) 70 eV electron ionization (EI) and pentaquadrupole triple-stage sequential ion-molecule reaction/CID product ion mass spectra. The results exemplify the superior ability of combined chemometric analysis and sequential mass spectrometric techniques, which benefits from both characteristic ion chemical reactivity and dissociation behavior, for rapid and accurate quantitation of complex isomeric mixtures.     

Intrinsic gas-phase electrophilic reactivity of cyclic N-alkyl- and N-acyliminium ions

The intrinsic gas-phase reactivity of cyclic N-alkyl- and N-acyliminium ions toward addition of allyltrimethylsilane (ATMS) has been compared using MS(2) and MS(3) pentaquadrupole mass spectrometric experiments. An order of electrophilic reactivity has been derived and found to agree with orders of overall reactivity in solution. The prototype five-membered ring N-alkyliminium ion 1a and its N-CH(3) analogue 1b, as well as their six-membered ring analogues 1c and 1d, lack N-acyl activation and they are, accordingly, inert toward ATMS addition. The five- and six-membered ring N-acyliminium ions with N-COCH(3) exocycclic groups, 3a and 3b, respectively, are also not very reactive. The N-acyliminium ions 2a and 2c, with s-trans locked endocyclic N-carbonyl groups, are the most reactive followed closely by 3c and 3d with exocyclic (and unlocked) N-CO(2)CH(3) groups. The five-membered ring N-acyliminium ions are more reactive than their six-membered ring analogues, that is: 2a > 2c and 3c > 3d. In contrast with the high reactivity of 2a, its N-CH(3) analogue 2b is inert toward ATMS addition. For the first time, the transient intermediates of a Mannich-type condensation reaction were isolated-the beta-silyl cations formed by ATMS addition to N-acyliminium ions-and their intrinsic gas-phase behavior toward dissociation and reaction with a nucleophile investigated. When collisionally activated, the beta-silyl cations dissociate preferentially by Grob fragmentation, that is, by retro-addition. With pyridine, they react competitively and to variable extents by proton transfer and by trimethylsilylium ion abstraction-the final and key step postulated for alpha-amidoalkylation. Becke3LYP/6-311G(d,p) reaction energetics, charge densities on the electrophilic C-2 site, and AM1 LUMO energies have been used to rationalize the order of intrinsic gas-phase electrophilic reactivity of cyclic iminium and N-acyliminium ions.