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- W1601164974 abstract "The trans-chloropalladation of disubstituted alkynes is a simple and efficient method for the construction of various types of pincer palladacycles that cannot be prepared or are easily available from other synthetic methods such as C−H bond activation and oxidative addition or transmetallation. In particular, various functional donor groups can be introduced in the metallated fragment–– such as, amines, pyridine, thioethers, phosphines, and phosphinites. This method allows the preparation of totally flat compounds that possess important photophysical properties in the solid state at room temperature. The chapter explains that pincer complexes, which contain both N- and P-donor groups, are among the most efficient catalyst precursors that promote the coupling reaction involving less reactive chloro-arenes. In view of the large number and variety of disubstituted alkynes that are easily prepared from a plethora of methods and that may undergo the halopalladation reaction, the number of tailor-made pincer-type palladacycles with specific properties is almost endless." @default.
- W1601164974 created "2016-06-24" @default.
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- W1601164974 creator A5080812341 @default.
- W1601164974 date "2007-01-01" @default.
- W1601164974 modified "2023-10-14" @default.
- W1601164974 title "Organometallic pincer-type complexes: recent applications in synthesis and catalysis" @default.
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- W1601164974 doi "https://doi.org/10.1016/b978-044453138-4/50002-7" @default.
- W1601164974 hasPublicationYear "2007" @default.
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