Printing PPEs: Fundamental Structure-Property Relationships.

A series of differentially alkyl- and alkoxy-substituted poly(-pheneyleneethynylene)s of different molecular weight were prepared and their rheological properties investigated. It was found that the side chain structure of the PPEs of roughly equal molecular weight and degree of polymerization has a significant influence on the rheology and printing behavior of the PPEs. Introduction of branched alkoxy or alkyl substituents improve the printing behavior of the PPEs dramatically.

Porous polymers based on aryleneethynylene building blocks.

Porous conjugated polymers are synthesized by metal-catalyzed coupling reactions. The progress for porous polymers when planar or tetrahedral building blocks are connected by alkyne units into novel materials is highlighted. The most prominent reaction for the buildup of the microporous alkyne-bridged polymers is the Sonogashira reaction, connecting alkynes to aromatic iodides or bromides.

Gold vinylidene complexes: intermolecular C(sp3)-H insertions and cyclopropanations pathways.

Highly reactive gold vinylidene species are used for intermolecular C(sp(3))-H insertions into unactivated alkanes (see scheme). In addition, they can be regarded as synthons for alkylidene carbenes. Initiated by cyclopropanation of the vinylidene species/alkylidene carbenoide, cyclobutene derivatives are formed in a diastereoselective fashion by a ring-enlargement cascade in only one step.

Influence of different light curing units on the cytotoxicity of various dental composites.

Objectives: To evaluate the dependence of the toxicity of various dental composites on the use of high- and low-power light curing units (LCUs).

Methods: The composites Filtek Z 250, Durafill VS, Solitaire 2 and Grandio were polymerized using different light densities from three LCUs, namely Heliolux II, Swiss Master Light (SML) and a prototype LED. The toxicity of polymerized samples was tested by exposing them to the cell culture medium up to 28 days.