Synthesis and complex formation of substituted amino-2-naphthylglyoximes of unsymmetrical vic-dioximes

Küçük Resim Yok

Tarih

2003

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Erişim Hakkı

info:eu-repo/semantics/closedAccess

Özet

anti-2-Naphthylchloroglyoxime has been synthesized by chlorination of anti-2-naphthylglyoxime. Reaction with aryl-or arylalkylamines in EtOH between 15°C and 20°C gives unsymmetrical vic-dioximes, namely, anilino-2-naphthylglyoxime (L1H2), benzylamino-2-naphthylglyoxime (L2H2), p-toluidino-2-naphthylglyoxime (L3H2) 1-naphthylamino-2-naphthylglyoxime (L4H2). The Ni(II) and Cu(II) complexes of these ligands are square-planar while the Co(II) complexes are octahedral with water molecules as axial ligands. 1H NMR, IR and elemental analyses data of the complexes and ligands are discussed.

Açıklama

Anahtar Kelimeler

Kaynak

Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry

WoS Q Değeri

Q4

Scopus Q Değeri

N/A

Cilt

33

Sayı

5

Künye