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Aldehydes spectroscopic properties

Conversion of acyl chlorides to aldehydes occurs upon reaction with HOTf and [Cp(CO)3WH] [32]. The reaction of HOTf with benzoyl chloride and [Cp(CO)3WH] led to the isolation of [Cp(CO)3W(PhCHO)]+OTf (Eq. (25)), in which the aldehyde is bound to the metal [32]. The spectroscopic properties and... [Pg.172]

The submitters obtained 8.68 g (96%). The aldehyde 4 should be used immediately after preparation. It cannot be purified by chromatography. The checkers observed the following physical and spectroscopic properties of 4 [a]p° (EtOAc, c 1.0)... [Pg.259]

For simple carbonyl compounds, the equilibrium between an aldehyde or a ketone and its corresponding enol is usually so shifted towards the keto form that the amount of enol at equilibrium can neither be measured nor detected by spectroscopy. Nevertheless, as recently emphasised by Hart (1979), this does not mean that the enol cannot exist free, not in equilibrium with ketones and aldehydes. Several examples of kinetically stable enols in the gas phase or in aprotic solvents have been reported. Broadly speaking, it appears that enols have relatively large life-times when they are prepared in proton-free media [e.g. the half-life of acetone enol was reported to be 14 s in acetonitrile (Laroff and Fischer, 1973 Blank et al., 1975) and 200 s in the gas phase (MacMillan et al., 1964)]. These life-times are related to an enhanced intramolecular rearrangement, indicated by the very high energies of activation (85 kcal mol-1 for acetaldehyde-vinyl alcohol tautomerization) which have been calculated (Bouma et al., 1977 Klopman and Andreozzi, 1979) It has therefore been possible to determine most of the spectroscopic properties of simple enols [ H nmr,l3C nmr (CIDNP technique), IR and microwave spectra of vinyl alcohol... [Pg.43]

Evidence Concerning the Molybdenum Site. Despite considerable debate, there is at present a good deal of agreement as to the overall mode of functioning of xanthine oxidase (20, 65-70). Furthermore, the EPR spectroscopic properties indicate that the molybdenum sites in aldehyde oxidase and (to a somewhat lesser extent) sulfite oxidase are very similar in nature to that in xanthine oxidase. [Pg.365]

RetinalS. The structure and photophysics of rhodopsins are intimately related to the spectroscopic properties of their retiny1-polyene chromophore in its protein-free forms, such as the aldehyde (retinal), the alcohol (retinol or vitamin A), and the corresponding Schiff bases. Since most of the available spectroscopic information refers to retinal isomers (48-55), we shall first center the discussion on the aldehyde derivatives. Three bands, a main one (I) around 380 nm and two weaker transitions at 280 nm and 250 nm (II and III), dominate the spectrum of retinals in the visible and near ultraviolet (Fig. 2). Assignments of these transitions are commonly made in terms of the lowest tt, tt excited states of linear polyenes, the spectroscopic theories of which have been extensively discussed in the past decade (56-60). In terms of the idealized C2h point group of, for example, all-trans butadiene, transitions are expected from the Ta ground state to B , A, and A" excited states... [Pg.105]

Spectroscopic Properties. Characteristic aldehyde absorptions are summarized in Table 3. A carbonyl stretching frequency between 1720 and ... [Pg.470]

Characterization of essential oils must include three kinds of analysis sensory analysis determination of physicochemical properties such as specific gravity (20°C), refractive index, optical rotation, aldehyde and carotenoid contents and solubility spectroscopic properties (UV and IR) and chromatographic analysis. In Table 5.10, the main analytical determinations that can be carried out in the quality control of essential oils are summarized. The ranges of values for each analytical parameter of essential oils from oranges are also shown. [Pg.179]

Original 1,2,4,5-tetrazines disubstituted by heterocyclic rings have been prepared and their electrochemical and spectroscopic properties studied <04NJC387>. A bowl-shaped neutral radical with a core annulene system bearing a verdazyl radical 47 has been synthesized in two steps from aldehyde 44 and carbazide derivative 45, as a stable solid in air <04OL1397>. [Pg.342]

The spectroscopic properties of these isomers are in accord with their formulation as the C-17 epimeric 0,X-diacetyl derivatives XV and XVI (R = OAc). Neither epimer exhibits aldehyde absorption in the IR-spectrum or aldehydic proton signals in the NMR-spectrum. Further,... [Pg.194]

Yanagida S, Ishimaru Y, Miyake Y, Shiragami T, Pac CJ, Hashimoto K, SakataT Semiconductor photocatalysis. 7. ZnS-catalyzed photoreduction of aldehydes and related derivatives 2-Electron-transfer reduction and relationship with spectroscopic properties. J Phys Chem 1989, 93(6) 2576—2582. [Pg.91]

Identification. The retention times on the HPLC system and the Rf-values on silica gel TLC of compounds 1 to and 1 2 to 2A agreed with those of the known carotenoids from Anacystis nidulans and Chromatium vinosum, respectively. Spectroscopic properties, molecular weights and number of hydroxyl groups, all of which are primary and/or secondary, are shown in TABLE 1. Assignments of H-NMR spectra of 2 "to 6 and 8 to 11 were made by comparison with the data of typical carotenoids. The CD spectra indicated that the absolute configuration of the hydroxyl groups at C-2 and C-3 were 2R and 3R, respectively. The position of the aldehyde group in IjO was analyzed with the EI-MS spectrum [3,4] ... [Pg.1008]

Although the enzyme itself has not been isolated, heme compounds with the spectroscopic properties of Atmungsferment have been isolated from various sources, including the snail Spirographis spallanzanii, heart mus-cle,i66 i67 and Corynebacterium diphtheriae Spirographis hemin differs from protohemin in the presence of a formyl group instead of the vinyl group in position Heart muscle and Corynebacterium hemin a also possess an aldehyde side chain which has not been further identified. [Pg.317]

Introduction Nomenclature Physical properties Spectroscopic properties Interesting aldehydes and ketones... [Pg.774]

Several studies have tackled the structure of the diketopiperazine 1 in the solid state by spectroscopic and computational methods [38, 41, 42]. De Vries et al. studied the conformation of the diketopiperazine 1 by NMR in a mixture of benzene and mandelonitrile, thus mimicking reaction conditions [43]. North et al. observed that the diketopiperazine 1 catalyzes the air oxidation of benzaldehyde to benzoic acid in the presence of light [44]. In the latter study oxidation catalysis was interpreted to arise via a His-aldehyde aminol intermediate, common to both hydrocyanation and oxidation catalysis. It seems that the preferred conformation of 1 in the solid state resembles that of 1 in homogeneous solution, i.e. the phenyl substituent of Phe is folded over the diketopiperazine ring (H, Scheme 6.4). Several transition state models have been proposed. To date, it seems that the proposal by Hua et al. [45], modified by North [2a] (J, Scheme 6.4) best combines all the experimentally determined features. In this model, catalysis is effected by a diketopiperazine dimer and depends on the proton-relay properties of histidine (imidazole). R -OH represents the alcohol functionality of either a product cyanohydrin molecule or other hydroxylic components/additives. The close proximity of both R1-OH and the substrate aldehyde R2-CHO accounts for the stereochemical induction exerted by RfOH, and thus effects the asymmetric autocatalysis mentioned earlier. [Pg.134]


See other pages where Aldehydes spectroscopic properties is mentioned: [Pg.470]    [Pg.473]    [Pg.209]    [Pg.18]    [Pg.473]    [Pg.74]    [Pg.75]    [Pg.98]    [Pg.119]    [Pg.470]    [Pg.473]    [Pg.427]    [Pg.58]    [Pg.183]    [Pg.753]    [Pg.753]    [Pg.755]    [Pg.1203]    [Pg.93]    [Pg.59]    [Pg.91]    [Pg.762]    [Pg.763]    [Pg.741]    [Pg.741]    [Pg.743]    [Pg.745]    [Pg.29]    [Pg.807]    [Pg.30]    [Pg.1014]   
See also in sourсe #XX -- [ Pg.753 , Pg.756 ]

See also in sourсe #XX -- [ Pg.762 , Pg.763 ]

See also in sourсe #XX -- [ Pg.741 , Pg.742 , Pg.743 , Pg.744 , Pg.745 , Pg.746 ]




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