This website uses cookies to give you the best user experience. If you continue without changing your settings we'll assume you are happy to receive all RSC cookies. You can change your cookie settings by navigating to our Privacy and Cookies page and following the instructions. These instructions are also obtainable from the privacy link at the bottom of any RSC page.
Lite Version|Standard version
Home > Chemical Communications >
To gain access to this content please
Log in via your home Institution.
Log in with your member or subscriber username and password.
Download


Buy PDF Add PDF to Basket (£42.50*)
*Exclusive of taxes
This article contains 3 page(s)
Abstract | Cited by

Recrystallisation of Ag[L1] (HL1 = 3{5}-[pyrid-2-yl]-5{3}-tert-butylpyrazole) in the presence of halide anions leads to two polymorphs of [Ag3(μ-Br)(μ-L1)2], which differ in their mode of supramolecular association, and the cluster [Ag10(μ-L1)8]Cl2. In contrast, Ag[L2] (HL2 = 3{5}-[isoquinol-1-yl]-5{3}-tert-butyl-pyrazole) crystallises as a cyclic tetrameric molecule.

Graphical abstract: New insights into the aggregation of silver pyrazolides using sterically hindered bidentate pyrazole ligands

Page: ^ Top


Enter Keywords, author, title,reference, or DOI
Log in | Register