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Solvents nuclear magnetic resonance spectra

Carborane, Bk>C2Hi2, is quite soluble in aromatic solvents and is sparingly soluble in aliphatic solvents. The infrared spectrum has been previously reported.25 The proton nuclear magnetic resonance spectrum of a chloroform-d3 solution of carborane contains a broad CH resonance at 6.46 t. [Pg.100]

Methylcarborane is an air-stable, white crystalline solid which is soluble in common organic solvents. The infrared spectrum (Nujol mull) contains major absorption bands at 3.90 (s), 8.83 (w), 9.12 (w), 9.69 (w), 9.83 (w), 10.03 (w), and 13.85 (s) p. The proton nuclear magnetic resonance spectrum of a carbon tetrachloride solution of methylcarborane contains a broad —CH resonance of intensity 1 at 6.52 r and a —CH3 resonance of intensity 3 at 8.02 r. [Pg.106]

The nuclear magnetic resonance spectrum of valproic acid as shown in Figure 4 was obtained on a Varian Associates T-60 NMR Spectrometer as a 10% w/v solution in a solvent of deuterated chloroform. The spectral peak assignments (2) are presented in Table II. [Pg.535]

Nuclear magnetic resonance spectrum (deuteriochloroform-solvent, internal tetramethylsilane reference) multiplet at... [Pg.26]

Using diethylene glycol diethyl ether, b.p. 188°, as the solvent, it has been shown from the nuclear magnetic resonance spectrum and infrared spectrum of the crudely distilled product that A,A, A"-trimethylborazine is obtained in comparable yield. However, the product cannot be separated efficiently from the solvent. [Pg.12]

Transfer the ether to a tared reaction tube and evaporate the solvent to leave crude triphenylmethane. Remove a sample for melting point determination and recrystallize the residue from an appropriate solvent, determined by experimentation. Prove to yourself that the compound isolated is indeed triphenylmethane. Obtain an infrared spectrum and a nuclear magnetic resonance spectrum. [Pg.333]

Nuclear magnetic resonance studies on meso-ionic l,2,4-triazol-3-ones (200) were used to examine their relationship to the alternative l,3,4-oxadiazol-2-imine structure (153). The effect of solvent polarity upon the ultraviolet spectrum of anhydro-3-hydroxy-1,4-diphenyl-1,2,4-triazolium hydroxide (200, R = = Ph, R = H) has been discussed... [Pg.45]

Nuclear magnetic resonance (NMR) spectroscopy is also largely used to characterize C02 complexes. The 13C NMR spectrum of C02 dissolved in a nonpolar solvent shows a resonance at 124ppm, which is shifted when C02 is bonded to a metal center. Depending on the mode of bonding, the shift may be up or down field, and may vary from a few ppm up to several hundreds of ppm. A few examples are given below for different types of bonding. [Pg.58]

With the exception of l,6-naphthyridin-8-ols, nuclear hdyroxy-1,6-naphthyridines would be expected to exist as the corresponding naphthyridinones. This has been confirmed by infrared,1035 ultraviolet,1026 and nuclear magnetic resonance spectral means.639 Other physicochemical studies of these oxy-1,6-naphthyridines include IR stretching frequencies1019 and ionization constants1040 of 1,6-naphthyr-idin-8-ols the mass spectra of 1,6-naphthyridinones the effect of solvents on the UV spectrum of an 8-hydroxy-1,6-naphthyridine derivative 773 and X-ray analysis of the dilactam, 4-hexyl-3,4,4a,5-tetrahydro-l,6-naphthyridine-2,7(l//,6Z/)-dione (1), in connection with its crystallization as self-assembled hydrogen-bonded polymers.549... [Pg.115]


See other pages where Solvents nuclear magnetic resonance spectra is mentioned: [Pg.104]    [Pg.108]    [Pg.109]    [Pg.75]    [Pg.26]    [Pg.22]    [Pg.50]    [Pg.104]    [Pg.108]    [Pg.476]    [Pg.307]    [Pg.19]    [Pg.364]    [Pg.379]    [Pg.42]    [Pg.221]    [Pg.629]    [Pg.17]    [Pg.221]    [Pg.97]    [Pg.82]    [Pg.13]    [Pg.933]    [Pg.1018]    [Pg.325]    [Pg.328]    [Pg.149]    [Pg.138]    [Pg.89]    [Pg.46]    [Pg.461]    [Pg.26]    [Pg.375]    [Pg.437]    [Pg.548]    [Pg.42]   


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Nuclear magnetic resonance solvents

Nuclear magnetic resonance spectra

Nuclear magnetic resonance spectra, solvent effects

Nuclear magnetic spectra

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Solvent effects on nuclear magnetic resonance spectra

Solvent resonance

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