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| 003 | ZW-GwMSU | ||
| 005 | 20250311093344.0 | ||
| 008 | 250311b |||||||| |||| 00| 0 eng d | ||
| 022 | _a09743626 | ||
| 040 |
_aMSU _bEnglish _cMSU _erda |
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| 050 | 0 | 0 | _aQD31 JOU |
| 100 | 1 |
_aMallick, Dibyendu _eauthor |
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| 245 | 1 | 0 |
_aStructural variations in aromatic 2π-electron three-membered rings of the main group elements / _ccreated by Dibyendu Mallick and Eluvathingal Jemmis |
| 264 | 1 |
_aBangalore : _bSprinter, _c2015. |
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| 336 |
_2rdacontent _atext _btxt |
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| 337 |
_2rdamedia _aunmediated _bn |
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| 338 |
_2rdacarrier _avolume _bnc |
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| 440 |
_aJournal of chemical sciences _vVolume 127, number 2, |
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| 520 | 3 | _aStructural variations of different 2 π-aromatic three-membered ring systems of main group elements, especially group 14 and 13 elements as compared to the classical description of cyclopropenyl cation has been reviewed in this article. The structures of heavier analogues as well as group 13 analogues of cyclopropenyl cation showed an emergence of dramatic structural patterns which do not conform to the general norms of carbon chemistry. Isolobal analogies between the main group fragments have been efficiently used to explain the peculiarities observed in these three-membered ring systems. | |
| 650 |
_aThree-membered ring _v2π-aromaticity _xIsolobal analogy |
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| 700 | 1 |
_aJemmis, Eluvathingal _eco author |
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| 856 | _uhttps://doi.org/10.1007/s12039-015-0777-2 | ||
| 942 |
_2lcc _cJA |
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| 999 |
_c169240 _d169240 |
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