Abstract
Nickel dithiolene complexes symmetrically appended with hydrogen-bond donor/acceptor functionalities such as imide, amide, or cyano/amide groups have been synthesized by a straightforward method of wide applicability starting from one single precursor. Single-crystal X-ray structures reveal the occurrence of one type of ribbon common to all compounds that is based on a recurrent self-complementary intermolecular hydrogen-bonded ring motif linking the symmetrically substituted complexes.
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