SCF-MO-untersuchungen der rotationskonformeren und dipolmomente aromatischer aldehyde

Klabuhn, B.; Clausen, Ernst; Goetz, Horst

doi:10.1016/0040-4020(73)80076-6

Cited by 14 publications

(1 citation statement)

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“…Quantum-chemical calculations in the p approximation of dipole moments of two planar conformers of a-and b-naphthaldehydes and a comparison of these values with the experimental values m did not lead to reliable conclusions about which form is favourable because of the similarity of the experimental and theoretical values. 154,155 The dipole moment of 2-naphthaldehyde (124) in CCl 4 (3.26 D) is smaller than that of its 1 : 1 complex with phenol (4.6 D). 156…”

Section: Dipole Momentsmentioning

confidence: 93%

Naphthaldehydes

Пожарский¹

2003

Russ. Chem. Rev.

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Data on methods for the preparation of naphthalde-Data on methods for the preparation of naphthaldehydes, their physicochemical properties, structural characteristics hydes, their physicochemical properties, structural characteristics and reactivities are generalised. Particular attention is given to and reactivities are generalised. Particular attention is given to procedures for formylation of naphthalenes and procedures for formylation of naphthalenes and peri peri-interactions -interactions involving the aldehyde group in the involving the aldehyde group in the a a-position. The bibliography -position. The bibliography includes 201 references includes 201 references. .

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Section: Dipole Momentsmentioning

confidence: 93%

Naphthaldehydes

Пожарский¹

2003

Russ. Chem. Rev.

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ChemInform Abstract: SCF‐MO‐UNTERSUCHUNGEN DER ROTATIONSKONFORMEREN UND DIPOLMOMENTE AROMATISCHER ALDEHYDE

Klabuhn¹,

Clausen²,

Goetz³

1973

Chemischer Informationsdienst

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Carbon‐13 NMR studies of substituted naphthalenes. I—complete assignments of the ¹³C chemical shifts with the aid of deuterated derivatives

1978

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Proton-coupled as well as noise-decoupled '"C NMR spectra of several substituted naphthalenes have been studied. Complete assignments of the ' " C signals based on selectively deuterated derivatives and on the '"C-'H coupling pattern have been made. For the methoxynaphthalenes, acetylnaphthalenes and naphthaldehydes the dominant conformations of the substituents have been deduced from the '"C chemical shifts.

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SCF-MO-untersuchungen der rotationskonformeren und dipolmomente aromatischer aldehyde

Cited by 14 publications

References 10 publications

Naphthaldehydes

Naphthaldehydes

ChemInform Abstract: SCF‐MO‐UNTERSUCHUNGEN DER ROTATIONSKONFORMEREN UND DIPOLMOMENTE AROMATISCHER ALDEHYDE

Carbon‐13 NMR studies of substituted naphthalenes. I—complete assignments of the ¹³C chemical shifts with the aid of deuterated derivatives

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SCF-MO-untersuchungen der rotationskonformeren und dipolmomente aromatischer aldehyde

Cited by 14 publications

References 10 publications

Naphthaldehydes

Naphthaldehydes

ChemInform Abstract: SCF‐MO‐UNTERSUCHUNGEN DER ROTATIONSKONFORMEREN UND DIPOLMOMENTE AROMATISCHER ALDEHYDE

Carbon‐13 NMR studies of substituted naphthalenes. I—complete assignments of the 13C chemical shifts with the aid of deuterated derivatives

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Carbon‐13 NMR studies of substituted naphthalenes. I—complete assignments of the ¹³C chemical shifts with the aid of deuterated derivatives