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A unique zigzag ⋅⋅⋅‐Bi‐Fe‐⋅⋅⋅ chain forms the basis of the structure of [nBuBiFe(CO)4]∞ (1; see picture), which was characterzized by single‐crystal X‐ray diffraction. Compound 1 was isolated from the ultrasonication of the dimeric product [{nBuBiFe(CO)4}2] from the reaction of [Et4N]3[Bi{Fe(CO)4}4] with nBuBr followed by acidification with HOAc.

ABSTRACT:The reaction of toluene diisocyanate with 2,2,3,3-tetrafluoro-1-propanol (fluoro compound) or 3-glycidoxypropyl trimethoxysilane(siloxane compound) and other additives to form the structure of the fluoro-based or siloxanebased polyurethane (PU) ionomer has been proven by infrared spectra. Experimental results indicated that the amount of water vapor permeability of the film made by fluoro-based or siloxane-based PU ionomer appeared to gradually increase with increasing concentration of the siloxane compound or fluoro compound, as a result of the formation of more porosities. Our experimental results also showed that the water vapor absorption was seen to be larger for the film made by siloxane-based PU ionomer film than for the film made by fluoro-based PU ionomer film, as a result of increased hydrophilic groups attached to the backbone of the PU ionomer molecule. For the film prepared by siloxane-based PU ionomer, both tensile strength and elongation appeared to increase with an increase in the concentration of siloxane compound. This may be the result of the intermolecular interaction between siloxane-based PU ionomer molecules themselves, thus enhancing the crosslinking capability of the ionomer molecules. On the other hand, both tensile strength and elongation for the film prepared by fluoro-based PU ionomer decreased with increasing concentration of the fluoro compound, as a result of intramolecular interaction greatly reducing the crosslinking capability of the ionomer molecules.

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