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Hydrogenation of hydroxy-substituted naphthalenes using Ru and Ni catalysts to desired decalols and decalindiols

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F19%3A43918080" target="_blank" >RIV/60461373:22310/19:43918080 - isvavai.cz</a>

  • Result on the web

    <a href="https://link.springer.com/content/pdf/10.1007/s11144-018-1504-z.pdf" target="_blank" >https://link.springer.com/content/pdf/10.1007/s11144-018-1504-z.pdf</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s11144-018-1504-z" target="_blank" >10.1007/s11144-018-1504-z</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Hydrogenation of hydroxy-substituted naphthalenes using Ru and Ni catalysts to desired decalols and decalindiols

  • Original language description

    The hydrogenation of mono or dihydroxynaphthalenes related to the position of hydroxyl groups was compared by terms of the reaction rate and the relative concentration of desired decalols resp. decalindiols in the reaction mixture under chosen reaction conditions (170 °C, 14 MPa) and using Ra–Ni catalyst with Cr promotor or 5% Ru/C catalyst. The amount of undesired hydrogenolytic products increased in the rows 2- &lt; 1-naphthol and 1,8- &lt; 2,7- &lt; 2,6- &lt; 1,5-dihydroxynaphthalene. The selective formation of decalin-1,5-diol in the concentration higher than 1% at the total conversion was not observed. Under suitable reaction conditions at the total conversion of starting substituted naphthalene, the highest achieved relative concentration of decalin-1,8-diol approximately 69% and 89% using Ru/C catalyst (Ru paste type 605) and Ra–Ni Acticat 1600 catalysts was achieved. © 2018, Akadémiai Kiadó, Budapest, Hungary.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10401 - Organic chemistry

Result continuities

  • Project

    <a href="/en/project/LO1613" target="_blank" >LO1613: Future materials</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2019

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Reaction Kinetics Mechanisms and Catalysis

  • ISSN

    1878-5190

  • e-ISSN

  • Volume of the periodical

    126

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    829-839

  • UT code for WoS article

    000463627000017

  • EID of the result in the Scopus database

    2-s2.0-85057345800