Computational studies of cyclobutadiene and benzocyclobutene fused to p- and o-quinone

MCKEE M., BALCI M., Kilic H., YURTSEVER E.

JOURNAL OF PHYSICAL CHEMISTRY A, cilt.102, sa.13, ss.2351-2356, 1998 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 102 Sayı: 13
  • Basım Tarihi: 1998
  • Doi Numarası: 10.1021/jp972966b
  • Dergi Adı: JOURNAL OF PHYSICAL CHEMISTRY A
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.2351-2356
  • Atatürk Üniversitesi Adresli: Evet

Özet

Cyclobutadiene and benzocyclobutenes fused to o- and p-quinone have been studied by computational methods. Geometries were optimized at the B3LYP/6-31G* level, and absolute NMR shielding values were calculated using the GIAO method with the HF/6-31G* basis set. NICS values of the compounds 8b,c and 9b,c indicate strong antiaromatic character for cyclobutadiene units. However, 8a and 9a show negative NICS values where the quinodal system reduces the antiaromaticity significantly by forcing these systems to possess a dimethylene-like structure. The calculated C-13 NMR chemical shifts of 6-9 and parent systems are in very good agreement with literature values.