Search

The FK506-FKBP12 binding domain of the kinase FRAP(FRB) forms a classic up-down four-helical bundle and the folding pathway of this protein is investigated using combination of equilibrium and kinetic studies. It is concluded that the four helical bundle proteins FRB populates an intermediate state during folding.

A chiral ferrocene-based boronic acid was interacted with (R)- and (S)-binol to produce two complexes that exhibited significantly different ferrocene-based electrode potentials. The differences in the redox behavior could be exploited to demonstrate in principle how high levels of enantiomeric excess in a mixture of enantiomers could be quantified and read-out using an electrochemical method.

Halide abstraction is shown to be a good method for the generation of mononuclear cationic complexes containing gallium donor ligands. The ligand properties are compared with related ten valance electron systems such as [N.sub.2], CO and BF.

While N2 and CO have played central roles in developing models of electronic structure, and their interactions with transition metals have been widely investigated, the valence isoelectronic diatomic molecules EX (E = group 13 element, X = group 17 element) have yet to be isolated under ambient conditions, either as the "free" molecule or as a ligand in a simple metal complex. As part of a program designed to address this deficiency, together with wider issues of the chemistry of cationic systems [LnM(ER)]+ (E = B, Al, Ga; A = aryl, amido, halide), we have targeted complexes of the type [LnM(GaX)]+ Halide abstraction is shown to be a viable method for the generation of mononuclear cationic complexes containing gallium donor ligands. The ability to isolate tractable two-coordinate products, however, is strongly dependent on the steric and electronic properties of the metal/ligand fragment. In the case of complexes containing ancillary ar-acceptor ligands such as CO, cationic complexes can only be isolated as base-trapped adducts, even with bulky aryl substituents at gallium. Base-free gallylene species such as [Cp*Fe(CO)2(GaMes)]+ can be identified only in the vapor phase by electrospray mass spectrometry experiments. With bis(phosphine) donor sets at the metal, the more favorable steric/electronic environment allows for the isolation of two-coordinate ligand systems, even with halide substituents at gallium. Thus, [Cp*Fe(dppe)(Gal)]+iBArf4]- (9) can be synthesized and shown crystallographically to feature a terminally bound Gal ligand; 9 represents the first experimental realization of a complex containing a valence isoelectronic group 13/group 17 analogue of CO and N2. DFT calculations reveal a relatively weakly bound Gal ligand, which is confirmed experimentally by the reaction of 9 with CO to give [Cp*Fe(dppe)+ (CO)]+[BArf4]-. In the absence of such reagents, 9 is stable for weeks in fluorobenzene solution, presumably reflecting (i) effective steric shielding of the gallium center by the ancillary phosphine and Cp* ligands; (ii) a net cationic charge which retards the tendency toward dimerization found for putative charge neutral systems; and (iii) (albeit relatively minor) population of the LUMOs of the Gal molecule through π overlap with the HOMO and HOMO-2 of the [Cp*Fe(dppe)]+ fragment. [ABSTRACT FROM AUTHOR]