Spectra indicating

Recent investigation of the effect of substituents in the para position of the phenylalanine ligand on the stability of the ternary complexes has revealed the secpience Br > OH > Q NH2 > H > F". Interestingly, analysis of CD spectra indicates a reduction of the arene-arene interaction" upon addition of 1,4-dioxane to aqueous solutions of the mixed-ligand complexes, in disagreement with previous observations by Sigel" . 

However, a second mole of alcohol or hemiformal caimot be added at the ordinary pH of such solutions. The equiUbrium constant for hemiformal formation depends on the nature of the R group of the alcohol. Using nmr spectroscopy, a group of alcohols including phenol has been examined in solution with formaldehyde (15,16). The spectra indicated the degree of hemiformal formation in the order of >methanol > benzyl alcohol >phenol. Hemiformal formation provides the mechanism of stabilization methanol is much more effective than phenol in this regard. 

Oxidation of azole anions can give neutral azole radicals which could, in principle, be tt (139) or a- (140) in nature. ESR spectra indicate structure (141 hyperfine splittings in G) for imidazolyl radicals, but both tt- and cr-character have been observed for pyrazolyl radicals. Tetrazolyl radicals (142 4 143) are also well known (79AHC(25)205). Oxidation of 2,4,5-triarylimidazole anions with bromine gives l,l -diimidazolyls (144) which are in equilibrium with the dissociated free radical (145) (70AHQ 12)103). 

Electron impact fragmentation studies on 1,2-benzisoxazoles and benzoxazole indicate that isomerization takes place before degradation. Shape analysis and metastable ion abundances in the mass spectra indicate that isomerization to o-cyanophenols occurred prior to degradation by loss of CO or NCH (75BSB207). 

A dication derived from 1,3,5,7-tetramethylcyclooctatetraene is formed at —78 C in SO2CI by reaction with SbFj. Both the proton and carbon NMR spectra indicate that the ion is a symmetrical, diamagnetic species, and the chemical shifts are consistent with an... 

Three different conformations are possible for monomeric chalcogen diimides (Eig. 10.1). Variable-temperature NMR spectra indicate that the cis,trans isomer of S(NR)2 is most stable in solution for small organic groups (R = Me, Bu). With bulkier organic substituents, small amounts of the trans,trans isomer exist in equilibrium with the cis,cis isomer. " The cis,cis isomer is observed in solutions of certain sulfur diimides with... 

Raman spectra, indicative of [M-M] + ions, are produced by the yellow glass obtained from the melt of Zn in ZnCl2 and also by the colourless, very moisture sensitive crystals of Cd2Al2Cls obtained from melts of Cd in CdCl2 and AICI3. X-ray studies show that the latter contains ethane-like [Cd2Cl6] groups with Cd-Cd reported as 257.6 pm and 256.1 pm " (cf 302 pm in the metal itself). The Cd nmr... 

Infrared and proton resonance spectra indicate that the tetrazine-dithione 223a exists in the dithione form shown. ... 

Our work demonstrates that EELS and in particular the combination of this technique with first principles electronic structure calculations are very powerful methods to study the bonding character in intermetallic alloys and study the alloying effects of ternary elements on the electronic structure. Our success in modelling spectra indicates the validity of our methodology of calculating spectra using the local density approximation and the single particle approach. 

According to different authors [28, 77, 78, 115], all compounds mentioned in Table 17 have isolated complexes TaFg3 or NbFg3 in their crystal structure. This is confirmed by similar IR absorption spectra indicating a strong band at -500 cm 1 for all such compounds [115, 119, 137, 138]. 

The electroluminescence spectra of the single-layer devices are depicted in Figure 16-40. For all these OPV5s, EL spectra coincided with the solid-state photoluminescence spectra, indicating that the same excited states are involved in both PL and EL. The broad luminescence spectrum for Ooct-OPV5-CN" is attributed to excimer emission (Section 16.3.1.4). 

During the reaction, protons are extracted from the brucite lattice. Infrared spectra [24, 25, 31] show that during charge the sharp hydroxyl band at 3644 cm" disappears. This absorption is replaced by a diffuse band at 3450 cm"1. The spectra indicate a hydrogen-bonded structure for ft-NiOOH with no free hydroxyl groups. ft-NiOOH probably has some adsorbed and absorbed water. However, TGA data... 

P NMR spectra indicate the T-shape geometry is retained in solution at -30°C but that the molecule is fluxional at room temperature. Rh(PPh3)3 undergoes a range of addition reactions with Lewis bases (CO, PF3, NH3) to afford various 16- and 18-electron species (Figure 2.14). 

The cis-structure (like [Rh(CO)2Cl]2 folded, with an angle of 123°) has been confirmed for PMe2Ph (X-ray) whereas the P(NMe2)3 analogue is trans (IR). Comparison of solid-state and solution IR spectra indicates that both isomers are present in solution (PR3 = PMe3, PMe2Ph, P(NMe2)3) [64],... 

It is an intensely reactive and hygoscopic yellow-brown substance (m.p. 75-78°C) its volatility suggests a low molecular mass Mossbauer spectra indicate 6-coordinate gold while the Raman spectrum is interpreted in terms of cw-bridged octahedral units. In the gas phase at 170°C, it comprises dimers and trimers [29] (electron diffraction). 

Vinylfuran did not polymerize with butyl lithium in hexane or tetrahydrofuran. Traces of resinous materials were isolated. Their spectra indicated complicated structures and not poly(2-vinylfuran). 

Diverse series of diphenyl sulphoxide (DPSO) complexes of Mn(II), Fe(II), Fe(III), Co(II), Ni(II), Cu(II), Zn(II), Ca(II), Al(II) and Mg(II) with various large anions have been reported187-191. The complexes have the general formula M(DPSO)6(Anion) where M is the metal cation. The reflection spectra in the visible and near-IR region indicate an octahedral configuration around the metal ion surrounded by the DPSO molecules. Comparison with the spectra of DMSO complexes shows that they have almost identical structures. IR spectra indicate that the oxygen atom in the sulphinyl group is the donor atom in all these complexes. 

Tschiersky and Baltes96 prepared di-D-fructose dianhydrides by heating fructose. Mass spectra of the permethyl ethers were obtained. Although the dianhydrides were of unknown structure, examination of the spectra indicate that all are difuranose dianhydrides (mlz 101 as the base peak, and low intensities of the ions mlz 88 and 277) and at least one is reminiscent of a 2,3-linked difuranose structure (relatively intense mlz 363 [M — 45]+).95-98... 

The second choice is a simpler solution. According to Sarko and Muggli,66 all 39 observed reflections in the Valonia X-ray pattern are indexable by a two-chain triclinic unit cell with a = 9.41, b =8.15 and c = 10.34 A, a = 90°, 3 = 57.5°, and y = 96.2°. Ramie cellulose, on the other hand, is completely consistent with the two-chain monoclinic unit cell. Also, there are significant differences between their high-resolution solid-state l3C NMR spectra, indicating that Valonia and ramie celluloses, the two most crystalline forms, reflect two distinct families of biosynthesis. On this basis, the Valonia triclinic and the ramie monoclinic forms are classified69 as Ia and Ip, respectively. It has been shown from a systematic analysis of the NMR spectra by these authors, and from electron-dif-... 

The molecules taking part in a valence tautomerization need not be equivalent. Thus, NMR spectra indicate that a true valence tautomerization exists at room temperature between the cycloheptatriene 110 and the norcaradiene (111). In this case one isomer (111) has the cw-l,2-divinylcyclopropane structure, while the other does not. In an analogous interconversion, benzene oxide and oxepin exist in a tautomeric equilibrium at room temperature. 

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