// Workers AI · dad joke modeWhat did Diimine say when it ran into an old friend? Mine to meet you.
Diimines are organic compounds containing two imine (RCH=NR') groups. Common derivatives are 1,2-diimines and 1,3-diimines. These compounds are used as ligands, but they are also precursors to other organic compounds.[1]
Preparation
[edit]Diimines are prepared by condensation reactions where a dialdehyde or diketone is treated with amine and water is eliminated.[2] Many are derived from the condensation of 1,2-diketones and dialdehydes with amines, often anilines.[3] The dialdehyde glyoxal is an especially common precursor. Similar methods are used to prepare Schiff bases and oximes.
1,2-Diimines
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The 1,2-diimines are also called α-diimines and 1,4-diazabutadienes. An example is glyoxal-bis(mesitylimine), a yellow solid that is synthesized by condensation of 2,4,6-trimethylaniline and glyoxal.[4][2] 2,2'-Bipyridine is a 1,2-diimine.
1,2-Diketimines are “non-innocent ligands”, akin to the dithiolenes.[5]
Synthesis of diiminopyridine complexes.
1,3-Diimines
[edit]For example, acetylacetone (2,4-pentanedione) and a primary alkyl- or arylamine will react, typically in acidified ethanol, to form a diketimine. 1,3-Diketimines are often referred to as HNacNac, a modification of the abbreviation Hacac for the conjugate acid of acetylacetone. These species form bidentate anionic ligands.
Uses
[edit]Substituted α-diimine ligands are useful in the preparation of post-metallocene catalysts, which are used for the polymerization of alkenes.[8][9]
1,2-Diimines are precursors to NHC ligands by condensation with formaldehyde.[4]
Reduction of 1,2-diimines gives diamines.[1]
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N,N'-di(propan-2-yl)ethane-1,2-diimine is a riot control agent that is synthesized by the condensation of glyoxal with isopropyl amine. Inhalation of 5mg can lead to irritation and congestion.[10]
References
[edit]- 1 2 Hans, Morgan; Delaude, Lionel (2010). "Microwave-Assisted Synthesis of 1,3-Dimesitylimidazolinium Chloride" (PDF). Organic Syntheses. 87: 77. doi:10.15227/orgsyn.087.0077.
- 1 2 Rodeschini, Vincent; Simpkins, Nigel S.; Zhang, Fengzhi (2007). "Chiral Lithium Amide Base Desymmetrization of a Ring Fused Imide: Formation of (3aS,7aS)-2-[2-(3,4-Dimethoxyphenyl)-ethyl]-1,3-dioxo-octahydro-isoindole-3a-carboxylic Acid Methyl Ester". Organic Syntheses. 84: 306. doi:10.15227/orgsyn.084.0306.
- ↑ Wang, F.; Chen, C. (2019). "A Continuing Legend: The Brookhart-Type α-Diimine Nickel and Palladium Catalysts" (PDF). Polymer Chemistry. 10 (19): 2354–2369. doi:10.1039/C9PY00226J.
- 1 2 Ison, Elon A.; Ison, Ana (2012). "Synthesis of Well-Defined Copper N-Heterocyclic Carbene Complexes and Their Use as Catalysts for a "Click Reaction": A Multistep Experiment That Emphasizes the Role of Catalysis in Green Chemistry". J. Chem. Educ. 89 (12): 1575–1577. Bibcode:2012JChEd..89.1575I. doi:10.1021/ed300243s.
- ↑ Mashima, Kazushi (2020). "Redox-Active α-Diimine Complexes of Early Transition Metals: From Bonding to Catalysis". Bulletin of the Chemical Society of Japan. 93 (6): 799–820. doi:10.1246/bcsj.20200056.
- ↑ Haaf, Michael; Schmedake, Thomas A.; West, Robert (2000-10-01). "Stable Silylenes". Accounts of Chemical Research. 33 (10): 704–714. doi:10.1021/ar950192g. ISSN 0001-4842. PMID 11041835.
- ↑ Asay, Matthew; Jones, Cameron; Driess, Matthias (2011-02-09). "N-Heterocyclic Carbene Analogues with Low-Valent Group 13 and Group 14 Elements: Syntheses, Structures, and Reactivities of a New Generation of Multitalented Ligands†". Chemical Reviews. 111 (2): 354–396. doi:10.1021/cr100216y. ISSN 0009-2665. PMID 21133370.
- ↑ Ittel, S. D.; Johnson, L. K.; Brookhart, M. (2000). "Late-Metal Catalysts for Ethylene Homo- and Copolymerization". Chemical Reviews. 100 (4): 1169–1203. doi:10.1021/cr9804644. PMID 11749263.
- ↑ Guo, Lihua; Dai, Shengyu; Sui, Xuelin; Chen, Changle (2016). "Palladium and Nickel Catalyzed Chain Walking Olefin Polymerization and Copolymerization". ACS Catalysis. 6: 428–441. doi:10.1021/acscatal.5b02426.
- ↑ Ellison, D. Hank (2007-08-24). Handbook of Chemical and Biological Warfare Agents, Second Edition. Boca Raton, Fla.: CRC Press. p. 63. ISBN 978-0-8493-1434-6.