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  1. No Access

    Chapter

    Die Zentralalpen östlich der Katschberglinie

    Wo die Gesteine der Schieferhülle am Ostrand des Tauernfensters unter das Unterostalpin der Linie Katschberg—Gmünd, markiert durch auf der Karte von M.F.Buchroithner (1984) ausgewiesene Hauptstörungen, abtauchen,...

    J. Zötl, E. Clar in Die Mineral- und Heilwässer Österreichs (1993)

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    Article

    Das vertikale Problem

    An verschiedenen Anomaliearten wurden die vertikalen Verhältnisse im Frontzahngebiet untersucht. Das Untersuchungsmaterial bestand aus Anfangsmodellen und den dazugehörigen Fernröntgenaufnahmen.

    G. Altuna, E. Clar, Dr. M. Freisfeld in Fortschritte der Kieferorthopädie (1973)

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    Article

    Literatur: Neue Bücher

    E. Schroll, F. Machatschki, E. Clar, A. Papp, W. E. Petrascheck in Mineralogy and Petrology (1965)

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    Article

    Literatur: Neue Bücher

    H. Wieseneder, F. Machatschki, E. Schroll in Tschermaks mineralogische und petrographis… (1964)

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    Book

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    Book

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    Chapter

    The Tautomerism of Phenols

    There is an increasing tendency to stabilize the dihydro structures in higher acenes. If phenols ketonize they transform their aromatic skeleton into the dihydro skeleton. Therefore the keto form must become t...

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    Hydrocarbons derived from 2.3,7.8-Di-(peri-naphthylene)-pyrene

    Pyrene (I) can be condensed twice with 1-bromonaphthalene in a sodium chloride—aluminium chloride melt to give 2.3,7.8-di-(peri-naphthylene)-pyrene which is separated from by-products by sublimation.1 ...

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    The Electrical Conductivity of Aromatic Hydrocarbons

    Graphite, the most highly condensed aromatic system, is a good conductor. This electrical conductivity originates in the mobility of the π-electrons in the molecular planes. In accordance with this the conduct...

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    Carbon Atoms, p-Electrons and Hybridization

    In wave mechanics, Bohr orbits are replaced by electron clouds. Thus an s-electron is represented by an electron cloud surrounding the nucleus and having a maximum intensity described by a ball or shell as indica...

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    Hydrocarbons derived from Quaterrylene

    Two molecules of perylene (I) condense in a sodium chloride—aluminium chloride melt at 150° to form quaterrylene (II) and a more readily soluble hydrocarbon as by-product.1

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    Quinquiphenyl and Sexiphenyl

    Quinquiphenyl and other polyphenyls are formed by reduction of benzenediazonium sulphate in concentrated sulphuric acid and acetic acid with formic acid and copper powder.1 A mixture of 4-iododiphenyl, 4-iodoterp...

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    Hydrocarbons Containing Four Five-membered Rings

    Diacenaphthylidene (I) is dehydrogenated by benzoquinone to (II) and two molecules of this resulting diene (II) condense with one molecule of benzoquinone to form the quinone (III).

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    Hydrocarbons derived from Anthanthrene

    Anthanthrene cannot be formulated with more than two benzenoid rings, each having one aromatic sextet as shown in formula (IV). It appears correct therefore to derive it in the same way from pyrene as anthrace...

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    Hydrocarbons derived from Terrylene

    1-Naphthyl magnesium bromide reacts with 2, 3-dichloro-1,4-naphthoquinone (I) to yield the diol (II). This is reduced to dinaphthyldichloronaphthalene (III) in boiling acetic acid with hydriodic acid. Cyclizat...

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    Magnetic Properties of Aromatic Hydrocarbons

    Hydrocarbons with paired electrons are diamagnetic. This means they are repelled in a magnetic field. This repulsion can be measured with a magnetic balance (Gouy’s method). The diamagnetic susceptibilities ar...

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    Nomenclature of Polycyclic Hydrocarbons

    There has never been any difficulty about the nomenclature of benzene and naphthalene derivatives. However, it was decades before a practical system for higher polycyclic hydrocarbons was developed. These latt...

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    The C—C Bond Length in Polycyclic Hydrocarbons

    The most important method for determining the C—C bond length in polycyclic hydrocarbons is X-ray analysis. When applied to benzene the length of a hexagon side was found to be 1·392 Å.1 If benzene were formed by...

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    The C=C Double Bond and Conjugation in Butadiene

    Another method of hybridization is the combination of a 2s-electron with two 2p-electrons. The sp 2 hybridization of the electrons of the two C-atoms forms the four C—H bonds plus the C—C single bo...

    E. Clar in Polycyclic Hydrocarbons (1964)

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    Chapter

    Hydrocarbons derived from Quaterphenyl

    Quaterphenyl is formed by pyrolysis if benzene is distilled through a glowing iron tube1 or over an electrically heated wire.2 4-Bromodiphenyl and sodium yield quaterphenyl3 as well as 4-iododiphenyl with copper ...

    E. Clar in Polycyclic Hydrocarbons (1964)

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