Reger Daniel L, Semeniuc Radu F, Smith Mark D
Department of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina, USA.
Dalton Trans. 2008 May 7(17):2253-60. doi: 10.1039/b719023a. Epub 2008 Mar 4.
The new ligand Ph(2)(O)POCH(2)C(pz)(3) (pz = pyrazolyl ring), prepared from the reaction of HOCH(2)C(pz)(3) and Ph(2)P(O)Cl in the presence of base, reacts with either AgBF(4) or Fe(BF(4))(2).6H(2)O in a 2/1 molar ratio to yield {Ph(2)(O)POCH(2)C(pz)(3)Ag}(BF(4)) () and {Ph(2)(O)POCH(2)C(pz)(3)Fe}(BF(4))(2) (), respectively. In the structure of , the silver is in an unusual planar geometry with each of the ligands in a kappa(2)-kappa(0) coordination mode. Slow evaporation of a thf solution of yields crystalline Ph(2)(O)POCH(2)C(pz)(3)Ag(thf)(2)}(BF(4))(2) (). In each cationic unit of , the two Ph(2)(O)POCH(2)C(pz)(3) ligands coordinate to the same two silver(i) centers in a kappa(2)-kappa(1) bonding mode, with a silver atom separation of 3.36 A. The supramolecular structure of both and is dominated by a pair of cooperative hydrogen bonding interactions between the Ph(2)P(O) secondary tecton and a hydrogen atom from a methylene group situated on a neighboring building block, which arranges the cations in chains. The reaction of HC(pz)(3) and AgO(3)SCF(3) (AgOTf) yields {HC(pz)(3)Ag(2)}(OTf)(2) (). The cationic unit in has a structure very similar to that of , but with a much shorter distance between the silver atoms at 2.86 A. The supramolecular structure of is dominated by an unusual pyrazolyl embrace interaction where the acceptor ring in the C-Hpi interaction is the pyrazolyl ring kappa(1)-bonded to silver in the adjacent dimeric unit rather than the other ring in a kappa(2)-bonded Cpz(2) unit. This interaction arranges the cations in chains which are further organized into sheets by the triflate anions that link the chains via combined AgO/CHO interactions. The iron in is octahedral with each tris(pyrazolyl)methane unit in the kappa(3)-tripodal coordination mode. The supramolecular structure is sheets formed by hydrogen bonding between the Ph(2)P(O) oxygen and a meta-position hydrogen on one of the diphenylphosphine rings from an adjacent cation.
新配体Ph₂(O)POCH₂C(pz)₃(pz = 吡唑基环)由HOCH₂C(pz)₃与Ph₂P(O)Cl在碱存在下反应制得,它与AgBF₄或Fe(BF₄)₂·6H₂O按2/1的摩尔比反应,分别生成{[Ph₂(O)POCH₂C(pz)₃]₂Ag}(BF₄)()和{[Ph₂(O)POCH₂C(pz)₃]₂Fe}(BF₄)₂()。在的结构中,银处于一种不寻常的平面几何构型,每个配体以κ²-κ⁰配位模式存在。四氢呋喃溶液缓慢蒸发得到结晶的[Ph₂(O)POCH₂C(pz)₃Ag]₂(thf)₂}(BF₄)₂()。在的每个阳离子单元中,两个Ph₂(O)POCH₂C(pz)₃配体以κ²-κ¹键合模式与相同的两个银(I)中心配位,银原子间距为3.36 Å。和的超分子结构均由二苯基磷酰基二级构造单元与相邻结构单元上亚甲基的氢原子之间的一对协同氢键相互作用主导,这些相互作用将阳离子排列成链。HC(pz)₃与AgO₃SCF₃(AgOTf)反应生成{[HC(pz)₃]₂Ag₂}(OTf)₂()。中的阳离子单元结构与非常相似,但银原子之间的距离短得多,为2.86 Å。的超分子结构由一种不寻常的吡唑基环抱相互作用主导,其中C-Hπ相互作用中的受体环是与相邻二聚体单元中银以κ¹键合的吡唑基环,而不是κ²键合的Cpz₂单元中的另一个环。这种相互作用将阳离子排列成链,三氟甲磺酸根阴离子通过AgO/CHO组合相互作用连接这些链,从而进一步将链组织成片层。中的铁呈八面体构型,每个三(吡唑基)甲烷单元以κ³-三脚架配位模式存在。超分子结构是由相邻阳离子中二苯基膦环上的Ph₂P(O)氧与间位氢之间的氢键形成的片层。