| Keyword search (4,163 papers available) | ![]() |
"Ottenwaelder X" Authored Publications:
| Title | Authors | PubMed ID | |
|---|---|---|---|
| 1 | Overlap and Covalency in a κN-Arylnitrosyl Cu(II) Metalloradical Formed by Hydroxylamine Oxidative Binding | MacKay A; Zsombor-Pindera J; Effaty F; Sheibany N; Gennarini F; Habibian M; Chen F; Askari MS; Brytskyi M; Kroeker S; Kennepohl P; Ottenwaelder X; | 41524899 CHEMBIOCHEM |
| 2 | Mechanochemistry for Metal-Organic Frameworks and Covalent-Organic Frameworks (MOFs, COFs): Methods, Materials, and Mechanisms | Marrett JM; Effaty F; Ottenwaelder X; Frišcic T; | 40708349 CHEMBIOCHEM |
| 3 | Mechanochemical Synthesis of Boroxine-linked Covalent Organic Frameworks | Hamzehpoor E; Effaty F; Borchers TH; Stein RS; Wahrhaftig-Lewis A; Ottenwaelder X; Frišcic T; Perepichka DF; | 38970305 CHEMBIOCHEM |
| 4 | Cooperative Sensitization Upconversion in Solution Dispersions of Co-Crystal Assemblies of Mononuclear Yb3+ and Eu3+ Complexes | Sun G; Xie Y; Wang Y; Mandl GA; Maurizio SL; Zhang H; Ottenwaelder X; Capobianco JA; Sun L; | 37040148 CNSR |
| 5 | Resonant acoustic mixing (RAM) for efficient mechanoredox catalysis without grinding or impact media | Effaty F; Gonnet L; Koenig SG; Nagapudi K; Ottenwaelder X; Frišcic T; | 36546478 CHEMBIOCHEM |
| 6 | Intramolecular H-bond stabilization of a primary hydroxylamine in salen-type metal complexes | Singh H; MacKay A; Sheibany N; Chen F; Mosser M; Rouet PÉ; Rousseau F; Askari MS; Ottenwaelder X; | 34545379 CHEMBIOCHEM |
| 7 | Programmed Synthesis of Tetra-Aryl Thiophenes with Stepwise, Ester-Controlled Regioselectivity | Messina C; Ottenwaelder X; Forgione P; | 34506149 CHEMBIOCHEM |
| 8 | Five Nitrogen Oxidation States from Nitro to Amine: Stabilization and Reactivity of a Metastable Arylhydroxylamine Complex. | Zsombor-Pindera J; Effaty F; Escomel L; Patrick B; Kennepohl P; Ottenwaelder X; | 33124796 CHEMBIOCHEM |
| 9 | Tuning Inner-Sphere Electron Transfer in a Series of Copper/Nitrosoarene Adducts. | Askari MS, Effaty F, Gennarini F, Orio M, Le Poul N, Ottenwaelder X | 32073833 CHEMBIOCHEM |
| 10 | A bio-inspired synthesis of oxindoles by catalytic aerobic dual C-H functionalization of phenols. | Huang Z, Askari MS, Esguerra KVN, Dai TY, Kwon O, Ottenwaelder X, Lumb JP | 29861988 CHEMISTRY |
| 11 | Synthesis of Highly Functionalized Triarylbismuthines by Functional Group Manipulation and Use in Palladium- and Copper-Catalyzed Arylation Reactions. | Hébert M, Petiot P, Benoit E, Dansereau J, Ahmad T, Le Roch A, Ottenwaelder X, Gagnon A | 27231755 CHEMBIOCHEM |
| 12 | Supramolecular control of monooxygenase reactivity in a copper(ii) cryptate. | Chaloner L, Khomutovskaya A, Thomas F, Ottenwaelder X | 27328176 CHEMBIOCHEM |
| Title: | Mechanochemistry for Metal-Organic Frameworks and Covalent-Organic Frameworks (MOFs, COFs): Methods, Materials, and Mechanisms | ||||
| Authors: | Marrett JM, Effaty F, Ottenwaelder X, Frišcic T | ||||
| Link: | https://pubmed.ncbi.nlm.nih.gov/40708349/ | ||||
| DOI: | 10.1002/adma.202418707 | ||||
| Publication: | Advanced materials (Deerfield Beach, Fla.) | ||||
| Keywords: | covalent organic frameworks; green chemistry; mechanisms; mechanochemistry; metal-organic frameworks; solvent‐; free; | ||||
| PMID: | 40708349 | Category: | Date Added: | 2025-07-25 | |
| Dept Affiliation: |
CHEMBIOCHEM
1 School of Chemistry, University of Birmingham, Edgbaston, Birmingham, B15 2TT, United Kingdom. 2 Department of Chemistry and Biochemistry, Concordia University, 7141 Sherbrooke St. W., Montreal, H4B 1R6, Canada. |
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Description: |
The mechanochemistry of metal-organic frameworks (MOFs) is a well-established field whose development has advanced the understanding and the design of both MOF materials and mechanochemical reactions. This review outlines the close and mutually beneficial interplay of these two fields over the past two decades, including the description of mechanochemical strategies to access MOFs as well as the response of these materials to mechanical treatment and/or stress. Furthermore, we highlight how the use of MOFs as model targets for mechanochemical synthesis simultaneously improves the accessibility and understanding of this class of materials and, conversely, advances the experimental and fundamental understanding of mechanochemical reactions. Similarly, we show the reciprocal benefits of comparing the mechanochemistry of organic molecular solids to that of MOFs. Finally, this review also portrays the rapid emergence of mechanochemistry of covalent-organic frameworks, a young area that promises to deliver new, rapid, efficient, solventless, and room-temperature access to these materials. |



