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Volumn 84, Issue 4, 2012, Pages 1101-1112

Antiaromatic ions and their value in quantifying aromaticity, as probes of delocalization, and potential as stable diradicals

Author keywords

Antiaromaticity; Aromaticity; Carbocations; Computational chemistry; Organic chemistry; Stability

Indexed keywords

ANTIAROMATICITY; AROMATIC SPECIES; AROMATICITIES; CARBOCATIONS; CORRESPONDING MEASURES; DELOCALIZATIONS; DIANIONS; DICATIONS; DIRADICALS; ENERGETIC PROPERTIES; NUCLEUS-INDEPENDENT CHEMICAL SHIFTS; ORGANIC CHEMISTRY; SENSITIVE PROBE; THEORETICAL TREATMENTS;

EID: 84859123282     PISSN: 00334545     EISSN: 13653075     Source Type: Journal    
DOI: 10.1351/PAC-CON-11-09-08     Document Type: Article
Times cited : (7)

References (38)
  • 15
    • 84859114195 scopus 로고    scopus 로고
    • Napthalene, phenanthrene, fluoranthrene, tropylium cation, cyclooctatetraene dication
    • Napthalene, phenanthrene, fluoranthrene, tropylium cation, cyclooctatetraene dication.
  • 17
    • 84859114198 scopus 로고    scopus 로고
    • Pentalene, 2, azulene dication, pyrene dication, 9-(1H-indenylidene)-9H-fluorene dication
    • Pentalene, 2, azulene dication, pyrene dication, 9-(1H-indenylidene)-9H-fluorene dication.
  • 33
    • 84859148021 scopus 로고    scopus 로고
    • Initial research on indenyldiene dications had revealed a tendency toward intramolecular cyclization, which could be avoided with a phenyl spacer to separate ring systems
    • Initial research on indenyldiene dications had revealed a tendency toward intramolecular cyclization, which could be avoided with a phenyl spacer to separate ring systems.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.