Complex emulsion inversion pattern associated with the partitioning of nonionic surfactant mixtures in the presence of alcohol cosurfactant

Commercial ethoxylated nonionic surfactant mixtures containing alcohol cosurfactant exhibit a three-phase behavior whose formulation strongly varies with the water/oil ratio. As a consequence, a change in water/oil ratio can result in a sequence of up to three different emulsion inversion processes, through a combination of formulation and composition effects.     

Cycloaddition reactions of 5-deutero-1-phenyl-4-vinylpyrazole. Stereoselectivecis “ene” reaction and simplification of NMR spectra of mixtures of cycloadducts

Summary The reaction of methyl propiolate (MP) with 1-phenyl-4-vinylpyrazole deuterated in the five position has clarified the¹H NMR spectrum of the mixture of the adducts 1:2 which are obtained as a result of a Diels-Alder cycloaddition followed by a non-regioselective ene reaction. The deuterated substrate allowed at the same time to establish the stereochemistry of the ene reaction as a concertedcis process.

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Cycloadditionsreaktionen von 5-Deutero-1-phenyl-4-vinylpyrazol. Stereoselektivecis-en-Reaktion und Vereinfachung von NMR-Spektren von Mischungen der Cycloaddukte (Kurze Mitt.)

Zusammenfassung Die Reaktion von Methylpropiolat (MP) mit an der 5-Stellung deuteriertem 1-Phenyl-4-vinylpyrazol wurde zur vereinfachten Interpretation der¹H-NMR-Spektren einer 1:2 Mischung von Addukten aus der Diels-Alder-Cycloaddition mit nachfolgender nicht-regioselektiver en-Reaktion eingesetzt. Das deuterierte Substrat erlaubte zugleich auch die Bestimmung der Stereochemie der en-Reaktion als einen konzertiertencis-Prozeß.

     

The nature of the AuI ... AuI Interactions between Cationic [AuL2]+ Complexes in the Solid State

The interaction energy of a [Au{C(NHMe)₂}₂]⁺ ... [Au{C(NHMe)₂}₂]⁺ dimer is investigated using the MP2 method and the LANL2DZ basis set when isolated or embedded in ionic an [Au{C(NHMe)₂}₂]₂anion₂ aggregate, a good model for the environment that these dimers feel in ionic crystals. A repulsive interaction energy is obtained when the dimer is isolated. However, it is possible to find short Au^I ... Au^I separations in [Au{C(NHMe)₂}₂]₂anion₂ aggregates, because in these aggregates the sum of the cation ... anion interactions overweight the sum of the cation ... cation plus anion...anion interactions. This explains why short Au^I ... Au^I separations are found in ionic crystals. The Au^I ... Au^I interaction found in [Au{C(NHMe)₂}₂]₂ anion₂ aggregates shows the same features observed in energetically stable dimers presenting Au^I... Au^I bonds. This makes appropriate to use the name counterion-mediated bonds for the Au^I... Au^I interactions found in [Au{C(NHMe)₂}₂]₂ anion₂ aggregates and ionic crystals.     

Polyfluorothiolate derivatives of rhodium(I). Crystal and molecular structure of [Rh(μ-SC6HF4)(C8H12)]2

Summary The thiolato-bridged dinuclear compounds [Rh(-SR)-(COD)]₂, where R=p-C₆HF₄ (1),p-C₆H₄F (2) and CF₃ (3), are obtained from the chloro-bridged analogue by ligand exchange.Compound (1) crystallizes in the space group P₁ with a=9.740(3)Å, b=11.642(4)Å, c=13.997(6)Å, =103.87(3)°, =106.98(3)° and =105.10(2)°; z=2. In this dinuclear molecule both Rh atoms have a square planar coordination sharing one edge, namely the two sulphur bridging atoms. The Rh—Rh separation of 2.96 Å is consistent with at most a very weak metal-metal interaction. Upon addition of CO the dimeric [Rh(-SR)(CO)₂]₂ (4), (5) and (6) are obtained, but addition of PPh₃ affords the monomeric species [Rh(SR)(PPh₃)-(COD)] (7), (8) and (9). Reactions of the dimeric tetracarbonyl derivatives with PPh₃ vary with the nature of R; [Rh(-SR)(PPh₃)(CO)]₂ is obtained when R=p-C₆H₄F (10) and CF₃ (11) but monomeric [Rh(SR)-(PPh₃)(CO)₂] (12) is produced when R=p-C₆HF₄. The latter mononuclear compounds, with R=p-C₆H₄F (13) and CF₃ (14), are also formed by reaction of [Rh(SR)-(PPh₃)(COD)] with CO.     

Benzylic cleavage and McLafferty rearrangement under electron ionization conditions in the fragmentation of 5,6-dialkyl-2, 4-diarylpyrimidines

Several 5,6-dialkyl-2,4-diarylpyrimidines were prepared and their electron ionization (EI) mass spectra reported. The benzylic cleavage takes place easily together with an important McLafferty rearrangement. The involvement of the nitrogen atom appears to be important in the fragmentation of 5-methyl-substituted pyrimidines. In contrast, the 6-methyl-substituted pyrimidines undergo benzylic cleavage without hydrogen transfer. Thus, the difference in the mass spectrometric behaviour allows the identification of these isomeric compounds which, in contrast, exhibit only small differences in their NMR spectra. Copyright 1999 John Wiley & Sons, Ltd.     

Convenient synthesis of nucleoside and isonucleoside analogues

[reaction: see text]. A very simple methodology to stereoselectively achieve tricyclic isonucleosides (nucleobase = thymine, uracil, and 5-fluoruracil) and 3'-C-branched nucleosides (nucleobase = theophylline) was performed by means of a DBU-mediated addition process using a readily available 2-bromo sugar. The mechanism for these transformations implies the loss of both substituents at C-2 and C-3 on the sugar moiety, and although it seems that DBU is probably involved, its involvement has not yet been ascertained. Cytosine did not react under these conditions.     

A pyrimidine thiolate Rh(I) complex: structure, bonding and one-dimensional interactions in solid and in solution

The reaction of [Rh(micro-Cl)(COD)]2 with 4,6-dimethyl-pyrimidinethiolate (Me2-pymt) and subsequent substitution of COD by CO yields [Rh(Me2-pymt)(CO)2]. The stacking pattern found in this compound is in contradiction with previously studied comparable square-planar complexes of type d8-[M(chelate)(monodentate)2] in which each ligand has different pi-acidic character. A theoretical study of the intermolecular interactions and conformation of the title compound has been carried out, combining semi-empirical band calculations on the real chains and ab initio(MP2 level) calculations on a model dimer. The combination of electronic and steric effects determines the rotation of the successive monomers and the deviation from linearity of the one-dimensional stacks. Its behaviour in solution is also special, developing a blue colour and forming micelles, when adding water to acetone solutions.     

Relaxation response of polymers containing highly flexible side groups monitored by broadband dielectric spectroscopy

The relaxation behavior of poly(5-acryloxymethyl-5-methyl-1,3-dioxacyclohexane), a polymer containing highly flexible side groups, is studied by broadband dielectric spectroscopy in the frequency and temperature ranges 10(-1)-10(9) Hz and 123-473 K, respectively. Above the glass transition temperature T(g) the dielectric loss in the frequency domain exhibits a prominent alpha absorption, followed in increasing order of frequencies by two secondary absorptions called beta and gamma. At temperatures slightly higher than T(g), the a relaxation is well separated from the beta, but as temperature increases overlapping between both relaxations augments forming an alphabeta absorption in the vicinity of 420 K. This latter absorption displays a shoulder on its high-frequency side corresponding to the y relaxation. The strength of the a relaxation decreases with increasing temperature, eventually vanishing at the temperature at which the alphabeta absorption is formed. The time retardation spectra of the isotherms are calculated and further used to facilitate the deconvolution of the overlapping relaxations. The fact that the temperature dependence of the beta relaxation also describes that of the alphabeta absorption suggests that both relaxations have the same nature. It seems that as temperature increases, the a relaxation feeds on the beta absorption until its complete disappearance. The gamma relaxation, in turn, seems to increase at the expense of the alphabeta process at high temperature.     

Selecting an agricultural technology package based on the flexible and interactive tradeoff method

Annals of Operations Research - The aim of this paper is to solve an agricultural technology packages selection problem by considering multiple dimensions which influence a maize producer’s...