Fourier 13C NMR and PMR including 13C satellites of oriented cyanopropyne

Fourier ¹³C and proton NMR spectra of cyanopropyne partially oriented by a nematic phase have been recorded and interpreted. It is shown that more accurate measurements are obtained much more rapidly by observing ¹³C satellites by Fourier PMR than by direct observation of the ¹³C spectrum. The geometry has been extracted from direct couplings; a small but systematic discrepancy with microwave spectroscopy is observed for the carboncarbon bond lengths.     

13C NMR-spectroscopy of polymethoxyxanthones

The ¹³C NMR chemical shifts of eight methoxy-xanthones are reported. Methoxy substituent effects depending on substituent position as well as on shielded ring carbon position have been evaluated. Methoxy substituent increments for xanthones are proposed.     

13C NMR of pterocarpans

¹³CNMR spectra of eight pterocarpans are reported Assignments are based on multiplicities and second-order features in off-resonance decoupled spectra and on chemical shifts in model compounds. Comparison of the degree of long-range (C, H) coupling in ¹H-coupled spectra is found useful     

13C separation by IRMPD of CF2HCL molecules with a powerful CO2-TEA laser

The single pulse separation parameters in IRMPD of CF₂HCL molecules have been obtained in relation with the laser fluence, the number of laser pulses, and the gas pressure. The measurements have been carried out using a fixed laser line (9P22) and an ordinary shape of the laser pulses.     

13C NMR study of propene dimerization on NiO/SiO2 catalysts

¹³C NMR studies of propene adsorbed on NiO/SiO₂ catalysts show -complex formation for propene with Ni²⁺ ions at low temperatures. Via a coordinative mechanism, 4-methylpentenes and, to a lower extent, 1-hexene are formed. No other isomers are formed as primary products but only via isomerization of the primary products.

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¹³C , NiO/SiO₂ - Ni²⁺ . 4- 1- . .

     

Biosynthese de la botryodiplodine,mycotoxine de penicillium roqueforti: Incorporations d'acetate[1-13C], [2-13C], [1-2 13C]et d'acide orsellinique 2-13C-carboxyle 13C], [3-4 13C]

Incorporations of [1-¹³C], [2-¹³C], [1-2¹³C]acetate and [2-¹³C, carboxyl-¹³C], [3-4¹³C]orsellinic acid into botryodiplodin indicate that this mycotoxin is biosynthesized by the polyketide pathway. Orsellinic acid is a precursor of botryodiplodin. A biosynthetic pathway, using orsellinic acid as precursor, is proposed.     

13C NMR spectrum of coumarin

Summary The positions of the signals from the C₃, C₅, C₆, and C₇ carbon atoms in the¹³C NMR spectrum of coumarin have been established with the aid of information obtained from the¹³C NMR spectra of [3-D]-, [4-D]-, and 7-methoxycoumarins and by the use of an additive calculation based on the increments of the methoxy group in the¹³C NMR spectrum of anisole.M. V. Lomonosov Moscow State University Scientific-Research Institute of Pharmacology, Academy of Medical Sciences of the USSR. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 458–462, July–August, 1975.     

Microwave spectra of tetrahydroselenophene-α13C, -β13C and molecular ring structure

Microwave spectra of isotopic species α-¹³C and β-¹³C of tetrahydroselenophene molecules have been investigated and rotational constants determined: A = 5608.98 Mc, B = 2819.532 Mc, C = 2022.624 Mc forα-¹³C isotopic species and A = 5695.94 Mc, B = 2770.714 Mc, C = 2009.166 Mc for β-¹³C isotopic species. The r_s-ring structure was found to be Se-C₂ = 1.963 Å, C₂-C₃ = 1.549 Å, C₃-C₄ = 1.527 Å, ∠C₅SeC₂ = 90° 44', ∠SeC₂C₃ = 104° 58', ∠C₂C₃C₄ = 106° 52', the angle of twist = 29° 44'.     

13C NMR spectroscopy of cyclopentenpoliols

The ¹³C NMR spectral parameters of eleven cyclopentenpoliols are discussed. Chemical shift criteria to distinguish isomeric 3' and 4' monodeoxy eucommiols have been clearly established.     

13C NMR studies of the interaction of CO with H2 over Rh/La2O3 catalyst

¹³C NMR studies have revealed that the interaction of CO with H₂ over a Rh/La₂O₃ catalyst yields surface particles containing carbonyl groups. Depending on the CO/H₂ ratio, carbonyl groups transform to various products: either alcohols and ethers or acids and esters.

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¹³C , CO H₂ Rh/La₂O₃ , . CO H₂ : .

     

29Si and 13C NMR spectra of permethylpolysilanes

²⁹Si, ¹³C and ¹H NMR spectra are reported for the series of linear permethylpolysilanes Me(SiMe₂)_nMe where n = 1 to 6, for the cyclic permethylpolysilanes (Me₂Si)_n where n = 5 to 8, and for a few related compounds. For linear polysilanes the ²⁹Si and ¹³C chemical shifts can be accurately calculated from simple additivity relationships based on the number of silicon atoms in α, β, γ and δ positions. Adjacent (α) silicon atoms lead to upfield shifts in the ²⁹Si and ¹³C resonances, whereas more remote silicon atoms lead to downfield shifts. The ²⁹Si chemical shifts of the polysilane chains are linearly related to the ¹³C shifts of the carbon atoms attached to the silicon. The ²⁹Si and ¹³C resonances of the cyclic silanes deviate from this relationship. Ring current effects arising from σ delocalization are suggested as an explanation for the deviations. Proton-coupled ²⁹Si NMR spectra are reported for Me₃SiSiMe₃ and for (Me₂Si)_n, n = 5 to 7.     

Vibrational relaxation of CO2(0001) in pure CO2

The rate constant for collisional deactivation of CO₂(00⁰1) in pure CO₂ has been measured at room temperature using the laser fluorescence technique. The relaxation rate has been found to be (1.0 ± 0.2) × 10^?14 cm³ s^?1 which is in favorable agreement with previously published values.     

13C13C spin spin coupling constants in azulenes

[4-¹³C]- Azulene and [4-¹³C]-4-methylazulene have been synthesized. The ¹³C¹³C spin coupling constants have been measured and interpreted in terms of πMO theory.     

Triatom-triatom collisions: Fixed angle close-coupling study of vibrational excitation in the 12CO2+13CO2 system

A close-coupling approach to the calculation of quantal vibrational transition probabilities for the fixed angle scattering of a linear triatomic molecule with another linear triatomic molecule is described. The method is applied to the ¹²CO₂+¹³C0₂ collisional system. For a calculated inelastic transition probability to have an appreciable magnitude, it is found that the amount of energy transferred in a transition must be very small and just one quantum of energy must be exchanged between either the symmetric stretch or the asymmetric stretch vibrational modes of ¹²C0₂ and ¹³CO₂. For collisional energies away from threshold, the probabilities for transitions involving the symmetric stretch ¹²CO₂ and ¹³CO₂ modes are insensitive to long range multipole terms in the potential energy surface, while the probabilities for energy exchange between the asymmetric stretch modes are considerably diminished when the long range terms are removed from the potential energy surface. A brief discussion is presented on the possibilities of extending the technique to the calculation of vibrational excitation cross sections for three-dimensional triato—triatom collisions.     

13C shielding tensors in p-alkoxybenzenes

All ¹³C shielding tensors in p-dimethoxybenzene and p-diethoxybenzene were determined from powder patterns by means of proton enhanced nuclear induction spectroscopy. In contrast to alkyl-substituted benzenes the tensor sets differ considerably at the various aromatic sites and all tensor elements at the two nonequivalent ortho positions are influenced by the asymmetric substituent. In the solid state p-diethoxybenzene was found to have a planar or nearly planar conformation, like p-dimethoxybenzene.     

13C-NMR spectra of fluorinated molecules using 19F-13C polarization transfer

¹³C-NMR spectra of fluorinated molecules are difficult to observe under conventional broad-band proton decoupling. The large coupling constants involved make polarization transfer between fluorine and carbon, using INEPT or DEPT experiments very effective while broad band fluorine decoupling collapses the multiplet pattern.     

Natural abundance 13C13C coupling constants observed via double quantum coherence. The two-dimensional ‘inadequate’ experiment for 13C NMR spectral analysis of erythronolide - B

A one- and a two-dimensional INADEQUATE NMR experiment afforded one-bond ¹³C¹³C coupling constants at natural abundance and total unambiguous signal assignment for erythronolide-B (1). ¹³C¹³C coupling constants at natural abundance and total unambiguous signal assignment for erythronolide-B (1).