CAJ | 학술논문

本文报道由于碘离子对不稳定的Ni(II)-S(芳基硫醇盐)键的亲核作用,使得Fe(CO)412和Ni(SR)2(dppe(SR=芳基硫醇盐)之间的反应生成NiI2(dppe).含碘和二芳基硫醇盐离子桥联的Ni-Ni双核配合物[(dppe)Ni(μ-I)(μ-pdt)Ni(dppe)]I和[(dppe)Ni(μ-I)(μ-edt)Ni(dppe)]I可方便地由[NiI2(dppe)]和[Ni(pdt)(dppe)]或[Ni(edt)(dppe)]在二氯甲烷的溶液中的反应制得;该类反应可认为是由于硫醇盐离子基团中S-供体上的孤对电子对Ni-I键的进攻所致.另一方面,我们观察到[FeCp(CO)2I]和[Ni(pdt)(dppe)]或[Ni(edt)(dppe)]在二氯甲烷中的反应极其缓慢;但当向上述反应体系中加入NH4PF6进行复分解置换后,源于碘离子和Ni(II)-S键的作用同样可得到含碘与二芳基硫醇盐离子桥联的Ni-Ni双核配合物[(dppe)Ni(μ-I)(μ-pdt)Ni(dppe)]PF6和 [(dppe)Ni(μ-I)(μ-edt)Ni(dppe)]PF6.实验结果说明在本文所讨认的镍(II)-硫醇盐离子-膦配合物中,Ni(II)-S键的反应活性随桥联的第二金属离子和不同的碘离子基元而改变.
본문보도유우전리자대불은정적Ni(II)-S(방기류순염)건적친핵작용,사득Fe(CO)412화Ni(SR)2(dppe(SR=방기류순염)지간적반응생성NiI2(dppe).함전화이방기류순염리자교련적Ni-Ni쌍핵배합물[(dppe)Ni(μ-I)(μ-pdt)Ni(dppe)]I화[(dppe)Ni(μ-I)(μ-edt)Ni(dppe)]I가방편지유[NiI2(dppe)]화[Ni(pdt)(dppe)]혹[Ni(edt)(dppe)]재이록갑완적용액중적반응제득;해류반응가인위시유우류순염리자기단중S-공체상적고대전자대Ni-I건적진공소치.령일방면,아문관찰도[FeCp(CO)2I]화[Ni(pdt)(dppe)]혹[Ni(edt)(dppe)]재이록갑완중적반응겁기완만;단당향상술반응체계중가입NH4PF6진행복분해치환후,원우전리자화Ni(II)-S건적작용동양가득도함전여이방기류순염리자교련적Ni-Ni쌍핵배합물[(dppe)Ni(μ-I)(μ-pdt)Ni(dppe)]PF6화 [(dppe)Ni(μ-I)(μ-edt)Ni(dppe)]PF6.실험결과설명재본문소토인적얼(II)-류순염리자-련배합물중,Ni(II)-S건적반응활성수교련적제이금속리자화불동적전리자기원이개변.
The reaction between Fe(CO)412 and Ni(SR)2(dppe) affords NiI2(dppe) due to the necleophilic attack of iodide on the labile N-S(aryl thiolate) bonds.The iodide-dithiolate-bridged binuclear Ni-Ni complexes[(dppe)Ni(μ-I)(μ-pdt)Ni(dppe)]I and[(dppe)Ni(μ-I)(μ-edt)Ni(dppe)]I can be readily prepared by reaction between[NiI2(dppe)]and[Ni(pdt)(dppe)] or[Ni(edt)(dppe)][dppe=1,2-bis (diphenyl phosphino)-ethane;pdt=1,3-propane-dithiolate;edt=1,2-ethane-dithiolate]in CH2C12 as a result of the attack on the Ni-I bond by the lone pairs of electrons on thiolato sulfur donors.On the other hand,the reaction between[FeCp(CO)2I] and [Ni(pdt)(dppe)] or[Ni(edt)(dppe)]in CH2C12 processes extremely slow.However, upon the metathesis with NH4PF6 for these reaction,the iodide-thiolate-bridged binuclear Ni-Ni complexes [(dppe)Ni(μ-I)(μ-pdt)Ni(dppe)]PF6 and [(dppe)Ni(μ-I)(μ-edt)Ni(dppe)]PF6 have been prepared due to the reaction of iodide and the Ni(II)-S bonds.These results suggest that the reactivity of Ni-SR bonds in such Ni-thiolate-phosphine complexes is tuneable with regard to the second metal ion and the different reactivity of iodide moiety.