Mechanochemistry as an emerging tool for molecular synthesis: what can it offer?
TL;DR: Mechanochemistry is becoming more widespread as a technique for molecular synthesis with new mechanochemical reactions being discovered at increasing frequency, and what more it can offer, aside from the clear benefit of reduced solvent consumption.
read more
Abstract: Mechanochemistry is becoming more widespread as a technique for molecular synthesis with new mechanochemical reactions being discovered at increasing frequency. Whilst mechanochemical methods are solvent free and can therefore lead to improved sustainability metrics, it is more likely that the significant differences between reaction outcomes, reaction selectivities and reduced reaction times will make it a technique of interest to synthetic chemists. Herein, we provide an overview of mechanochemistry reaction examples, with ‘direct’ comparators to solvent based reactions, which collectively seemingly show that solid state grinding can lead to reduced reaction times, different reaction outcomes in product selectivity and in some instances different reaction products, including products not accessible in solution.
read more
Chat with Paper
AI Agents for this Paper
Find similar papers on Google Scholar, PubMed and Arxiv
Write a critical review of this paper
Analyze citations of this paper to find unaddressed research gaps
Citations
3d Transition Metals for C-H Activation.
Parthasarathy Gandeepan,Thomas Müller,Daniel Zell,Gianpiero Cera,Svenja Warratz,Lutz Ackermann +5 more
TL;DR: A comprehensive overview on first row transition metal catalysts for C-H activation until summer 2018 is provided.
1.8K
Mechanochemistry for Synthesis
TL;DR: This mini-review examines the potential of mechanochemistry in chemical and materials synthesis, by providing a cross-section of the recent developments in using ball milling for the formation of molecules and materials based on covalent and coordination bonds.
857
Main group mechanochemistry: from curiosity to established protocols.
Davin Tan,Felipe García +1 more
TL;DR: This tutorial review turns the spotlight towards mechanochemical research in the field of inorganic main group chemistry, highlighting significant advantages that solid-state inorganic reactions often possess, and the potential for these to drive the development of greener methodologies within the modern main group arena.
Ball milling as a mechanochemical technology for fabrication of novel biochar nanomaterials.
Manish Kumar,Xinni Xiong,Zhonghao Wan,Yuqing Sun,Daniel C.W. Tsang,Juhi Gupta,Bin Gao,Xinde Cao,Jingchun Tang,Yong Sik Ok +9 more
TL;DR: This review critically evaluates the synthesis, characterization, and application of ball-milled biochar nanomaterials based on the latest findings and offers insights into opportunities and future prospects related to sustainable and facile synthesis of biochar-based novel materials for achieving sustainable development goals.
420
Sustainability Assessment of Mechanochemistry by Using the Twelve Principles of Green Chemistry.
TL;DR: In this article, the authors present a series of examples that will clearly illustrate how mechanochemistry can significantly contribute to the fulfillment of Green Chemistry in a more holistic manner, and demonstrate that mechanochemistry satisfies more than one of the principles of green chemistry.
416
References
Copper N-heterocyclic carbene complexes in catalysis
TL;DR: The ability of N-Heterocyclic carbene ligated copper (NHC) complexes to functionalize carbonyls, alkenes and alkynes is discussed in this paper.
A benzimidazole functionalised DO3A chelator showing pH switchable coordination modes with lanthanide ions
Christopher M. Fisher,Euan Fuller,Benjamin P. Burke,Vijetha Mogilireddy,Simon J. A. Pope,Amanda E. Sparke,Isabelle Déchamps-Olivier,Cyril Cadiou,Françoise Chuburu,Stephen Faulkner,Stephen J. Archibald +10 more
TL;DR: The benzimidazole DO3A chelator allows for sensitisation of europium, terbium and ytterbium luminescence by the heterocycle and also shows a pH dependent coordination change due to protonation of the chelator.
Solvent-free asymmetric aldol reaction organocatalyzed by (S)-proline-containing thiodipeptides under ball-milling conditions
TL;DR: Thiodipeptide (S,S)-1d catalyzed the stereoselective formation of the expected aldol products with excellent diastereo- and enantioselectivity and may be ascribed to the increased NeH acidity of the thioamide segment that leads to stronger H-bonding interaction with the aldehyde carbonyl at the transition state and thus higher stereoinduction.
Advances in elucidating mechanochemical complexities via implementation of a simple organic system.
Adam A. L. Michalchuk,Adam A. L. Michalchuk,Ivan A. Tumanov,Valeri A. Drebushchak,Elena V. Boldyreva +4 more
TL;DR: A model is described that may account for formation of a novel phase obtained through impact treatment of the simple organic system, α-glycine + β-malonic acid, and considering the formation and character of mechanically produced tablets.
Related Papers (5)
Jean-Louis Do,Tomislav Friščić +1 more