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Selective borane reduction of phosphinoferrocene carbaldehydes to phosphinoalcohol-borane adducts. The coordination behaviour of 1-(diphenylphosphino)-1 '-(methoxymethyl)ferrocene, a new ferrocene O,P-hybrid donor prepared from such an adduct

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F13%3A10133859" target="_blank" >RIV/00216208:11310/13:10133859 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1039/c2dt32511j" target="_blank" >http://dx.doi.org/10.1039/c2dt32511j</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c2dt32511j" target="_blank" >10.1039/c2dt32511j</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Selective borane reduction of phosphinoferrocene carbaldehydes to phosphinoalcohol-borane adducts. The coordination behaviour of 1-(diphenylphosphino)-1 '-(methoxymethyl)ferrocene, a new ferrocene O,P-hybrid donor prepared from such an adduct

  • Original language description

    The reduction of ferrocene phosphino-aldehydes, R2PfcCHO (R = Ph, 2; Cy, 3; fc = ferrocene-1,1'-diyl, Cy = cyclohexyl) and (S-p)-[Fe(eta(5)-C5H3-1-CHO-2-PPh2)(eta(5)-C5H5)] ((Sp)-4), with BH3*THF or BH3*SMe2 in THF at 0 degrees C selectively afforded thecorresponding phosphinoalcohol-borane adducts, R2PfcCH2OH*BH3 (R = Ph, 5; Cy, 6) and (Sp)-[Fe(eta(5)-C5H3-1-CH2OH-2-PPh2)(eta(5)-C5H5)]*BH3 ((Sp)-7), in quantitative yields. In contrast, the reactions performed at elevated temperatures favoured the formation of methyl derivatives (e. g., Ph2PfcCH3*BH3 (8)) resulting from overreduction (deoxygenation). The crystal structures of 3, 5, (Sp)-7, 8 and Cy2PfcBr (9) have been determined by single-crystal X-ray diffraction analysis. The crystal assemblies of adducts 5 and (Sp)-7 are built up by means of C-H...O contacts, O-H...HB dihydrogen bonds and other soft interactions but, surprisingly, not via the conventional O-H...O hydrogen bonds. Adduct 5 was smoothly deprotected to give the corresp

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CA - Inorganic chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GAP207%2F10%2F0176" target="_blank" >GAP207/10/0176: Homologous functional phosphinoferrocene ligands for coordination chemistry and catalysis</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Dalton Transactions

  • ISSN

    1477-9226

  • e-ISSN

  • Volume of the periodical

    42

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    17

  • Pages from-to

    3373-3389

  • UT code for WoS article

    000314783300014

  • EID of the result in the Scopus database