Carbon Insertion into arachno-6,9-C2B8H14 via Acyl Chlorides. Skeletal Alkylcarbonation (SAC) Reactions: A New Route for Tricarbollides
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F13%3A39896342" target="_blank" >RIV/00216275:25310/13:39896342 - isvavai.cz</a>
Alternative codes found
RIV/61388980:_____/13:00397293
Result on the web
<a href="http://pubs.acs.org/doi/abs/10.1021/ic401293g" target="_blank" >http://pubs.acs.org/doi/abs/10.1021/ic401293g</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/ic401293g" target="_blank" >10.1021/ic401293g</a>
Alternative languages
Result language
angličtina
Original language name
Carbon Insertion into arachno-6,9-C2B8H14 via Acyl Chlorides. Skeletal Alkylcarbonation (SAC) Reactions: A New Route for Tricarbollides
Original language description
Reactions between arachno-6,9-C2B8H14 (1) and selected acyl chlorides, RCOCl, in the presence of PS (PS = "proton sponge", 1,8-dimethylamino naphthalene) in CH2Cl2 for 24 h at reflux, followed by in situ acidification with concentrated H2SO4 at 0 degreesC, generate a series of neutral alkyl and aryl tricarbollides 8-R-nido-7,8,9-C3B8H11 (2) (where R = CH3, 2a; C2H5, 2b; n-C4H9, 2c; C6H5, 2d; 4-Cl-C6H4, 2e; 4-Br-C6H4, 2f; 4-I-C6H4, 2g; 1-C10H7, 2h; and 2-C10H7, 2i). The best yields were achieved for aryl derivatives (80-95%) while the yields of the corresponding alkyl substituted compounds are lower (60-70%). These skeletal alkylcarbonation (SAC) reactions are consistent with an aldol-type condensation between the RCO group and open-face hydrogen atomson the dicarbaborane 1, which is associated with the insertion of the carbonyl carbon atom into the structure of arachno-6,9-C2B8H14 (1) under elimination of three extra hydrogen atoms as H2O and HCl. The reactions thus result in an effe
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CA - Inorganic chemistry
OECD FORD branch
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Result continuities
Project
<a href="/en/project/GAP207%2F11%2F0705" target="_blank" >GAP207/11/0705: Carborane-modified iron-arene complexes</a><br>
Continuities
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
Inorganic Chemistry
ISSN
0020-1669
e-ISSN
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Volume of the periodical
52
Issue of the periodical within the volume
15
Country of publishing house
US - UNITED STATES
Number of pages
7
Pages from-to
9087-9093
UT code for WoS article
000322863300091
EID of the result in the Scopus database
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