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- W2893384132 endingPage "14598" @default.
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- W2893384132 abstract "Solid-state synthesis (S3) is an attractive approach to organic synthesis as in principle it offers minimal solvent waste and high yield. However, many functional groups are ill-suited for S3 reactions, which tend to only proceed when substrates are aligned in the solid-state according to the topochemical principle. The aim of this work is to use high yield, low-waste synthetic methods to develop a library of novel Schiff bases that can be utilized as linker ligands to prepare coordination networks. Herein, we report that eight pyridyl- and/or imidazolyl-substituted Schiff bases, 1–8, five of which are new chemical entities, can be prepared via reaction of an amine and an aldehyde without the use of solvent. All eight compounds were prepared via solvent-drop grinding (SDG) in multigram scale in >95% yield and each was characterized by FTIR, 1H and 13C NMR spectroscopies and single crystal X-ray diffraction. One of the aldehydes used is a liquid under ambient conditions so its reactions to form 1–4 are not..." @default.
- W2893384132 created "2018-10-05" @default.
- W2893384132 creator A5001382768 @default.
- W2893384132 creator A5019632748 @default.
- W2893384132 creator A5040708976 @default.
- W2893384132 creator A5078006809 @default.
- W2893384132 date "2018-09-29" @default.
- W2893384132 modified "2023-10-12" @default.
- W2893384132 title "High Yield, Low-Waste Synthesis of a Family of Pyridyl and Imidazolyl-Substituted Schiff Base Linker Ligands" @default.
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