Janczak Jan, Idemori Ynara Marina
Departamento de Química, Instituto de Ciências Exatas, Universidade Federal de Minas Gerais, CEP 31270-901 Belo Horizonte MG, Brazil.
Acta Crystallogr C. 2002 Jan;58(Pt 1):m23-5. doi: 10.1107/s0108270101017590. Epub 2001 Dec 14.
Crystals of a new antimony(III) phthalocyanine complex with the formula [Sb(C32H16N8)]4(Sb4I16), or (SbPc)4+*[Sb(4)I(16)]4-, where Pc is phthalocyaninate, have been obtained by the reaction of pure powdered antimony with phthalonitrile under a stream of iodine vapour. The crystals are built up from separate but interacting (SbPc)+ cations and centrosymmetric [Sb4I16]4- anions. Each Sb atom of two independent (SbPc)+ units is bonded to the four isoindole N atoms of the phthalocyaninate(2-) macrocycle and lies 1.0 A out of the plane defined by four isoindole N atoms. The anionic part of the complex consists of four SbI6 distorted octahedra joined together into a centrosymmetric [Sb4I16]4- anion. The arrangement of oppositely charged moieties in the crystal is mainly determined by ionic attraction and by a set of distinct donor-acceptor interactions between (SbPc)+ and [Sb4I16]4- ions.
一种新的锑(III)酞菁配合物晶体,其化学式为[Sb(C₃₂H₁₆N₈)]₄(Sb₄I₁₆),即(SbPc)₄⁺·[Sb₄I₁₆]⁴⁻(其中Pc为酞菁酸根),是通过纯锑粉与邻苯二甲腈在碘蒸气流下反应制得的。这些晶体由独立但相互作用的(SbPc)⁺阳离子和中心对称的[Sb₄I₁₆]⁴⁻阴离子构成。两个独立的(SbPc)⁺单元中的每个Sb原子都与酞菁酸根(2⁻)大环的四个异吲哚N原子键合,且位于由四个异吲哚N原子所定义平面之外1.0 Å处。该配合物的阴离子部分由四个SbI₆畸变八面体连接在一起形成中心对称的[Sb₄I₁₆]⁴⁻阴离子。晶体中带相反电荷部分的排列主要由离子吸引力以及(SbPc)⁺和[Sb₄I₁₆]⁴⁻离子之间一组独特的供体 - 受体相互作用决定。