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phenylene-1-bis[(triphenylphosphine)gold(I)]sulfonio-3-[(triphenylphosphine)gold(I)]thiolate tetrafluoroborate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

448280-28-2

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448280-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 448280-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,8,2,8 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 448280-28:
(8*4)+(7*4)+(6*8)+(5*2)+(4*8)+(3*0)+(2*2)+(1*8)=162
162 % 10 = 2
So 448280-28-2 is a valid CAS Registry Number.

448280-28-2Downstream Products

448280-28-2Relevant academic research and scientific papers

Aurophilicity-based one-dimensional arrays of gold(I) phenylene-1,3- and -1,4-dithiolates

Ehlich, Hendrik,Schier, Annette,Schmidbaur, Hubert

, p. 3721 - 3727 (2002)

Phenylene-1,3-dithiol is converted into a trinuclear gold complex by treatment with 1 equiv of {[(Ph3P)Au]3O}+BF4-. In the product, the phenylene unit bears one gold thiolate and one di(gold)sulfonium function. These components aggregate into one-dimensional arrays through head-to-tail aurophilic contacts between the two functions. In the association process, the Au-S-Au angle of the sulfonium group is opened up to accommodate the incoming gold atom between its metal centers. A similar mode of aggregation is found for the triply aurated biphenylene-4,4′-dithiol obtained using the tri(gold)oxonium salt with tri(p-tolyl)phosphine ligands. Probably for steric reasons, in this oligomerization process, the gold(I) thiolate unit is attached side-on to the digold sulfonium unit with retention of the small Au-S-Au angle. Under similar reaction conditions, and with the same molar ratio of the components, phenylene-1,4-dithiol is converted into the bis-sulfonium salt: 1,4-{[(p-Tol)3PAu]2S}2C6 H4(BF4)2, the dications of which also associate into chains. Along the chains, the phenylene spacers alternate with tetranuclear gold clusters which arise from intimate aggregation of pairs of gold atoms. Together with previous findings, the present results show that gold thiolate (-SAuL) and digold sulfonium functions [-S(AuL)2+] in proper orientation at an arene unit (α-ω) can be considered as soldering points which can be used for joining up the molecular units into one-dimensional arrays solely through metal-metal contacts, which appear to be operative even against Coulomb repulsion between cations. The reaction of biphenylene-4,4′-dithiol with 2 equiv of sodium methoxide and [tri-(c-hexyl)phosphine]gold chloride gives only neutral digold dithiolate complex 4 which is not associated owing to the steric bulk of the tri(c-hexyl)phosphine ligands.

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