Franco CecconiCarlo A. GhilardiStefano MidolliniAnnabella OrlandiniAlessandro Bencini
The mono- and di-cationic clusters [Co6(µ3-Te)8(PEt3)6][PF6]n(n= 1 2 or 2 3) have been prepared by oxidation of the uncharged species [Co6(µ3-Te)8(PEt3)6]1. The diamagnetic dicationic cluster has been fully characterized by a crystal structure determination: space group P21/c, a= 13.303(3), b= 19.043(3), c= 14.401(7)Å, β= 112.30(4)° and Z= 2. The cluster cation, which is isostructural with the other stellated octahedral members of the series [M6(µ3-E)8(PEt3)6]n+(E = S or Se), is significantly distorted, with Co–Co bond distances ranging from 3.005(2) to 3.265(2)Å. The magnetic behaviour of [Co6(µ3-Te)8(PEt3)6][PF6]2 is different from that of a BF4– salt previously reported.
Franco CecconiCarlo A. GhilardiStefano MidolliniAnnabella OrlandiniPiero ZanelloA. CinquantiniAlessandro BenciniMyriam G. UytterhoevenGianluca Giorgi
Judith A. BandyMalcolm L. H. GreenDermot O’Hare
Dieter FenskeJohannes OhmerKurt Merzweiler
Franco CecconiCarlo A. GhilardiStefano MidolliniAnnabella OrlandiniPiero Zanello
Günther ThieleZhiliang YouStefanie Dehnen