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|a 10.1021/acs.organomet.4c00263
|2 doi
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|a pubmed24n1533.xml
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|a (NLM)39268182
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Byrne, Paul
|e verfasserin
|4 aut
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|a Synthesis of a Palladium Dimer Supported by a C-Bound Trifluoroacetonate Bridge Formed by Cleavage of a Hexafluoroacetylacetonate Ligand
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|c 2024
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|a Text
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|a ƒaComputermedien
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|a ƒa Online-Ressource
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|a Date Revised 14.09.2024
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|a published: Electronic-eCollection
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|a Citation Status PubMed-not-MEDLINE
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|a © 2024 The Authors. Published by American Chemical Society.
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|a Palladium(II) hexafluoroacetylacetonate (Pd(Hfacac)2) is known to form adducts of bases, such as lutidine (2,6-dimethylpyridine). When treated with approximately 3 equiv of lutidine, Pd(Hfacac)2 yields a 1:1 complex as reported in the literature, Pd(O,O-Hfacac)(C-Hfacac)(lutidine), 1. However, when the amount of excess lutidine is increased, a new complex, 2, is formed. A single-crystal X-ray structure of 2 proves it is a rare example of a dimeric palladium complex containing two Pd(Hfacac)(lutidine) fragments bridged by a dianionic trifluoroacetonate ligand, μ-CHC(O)CF3. The formation of 2 is accompanied by a white precipitate determined to be a mixture of trans-Pd(O2CCF3)2(lutidine)2 (3), confirming the fate of the missing trifluoroacetate fragment from the cleavage of the Hfacac ligand, and [lutidinium][Hfacac] (4). Subsequent experiments revealed the determinative role that water played in this reaction. The mechanism of cleavage of the Hfacac ligand was explored by DFT methods
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|a Journal Article
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|a Burgoon, Hugh
|e verfasserin
|4 aut
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|a Koester, Jessica
|e verfasserin
|4 aut
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|a Chen, Wei-Yuan
|e verfasserin
|4 aut
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|a Ziegler, Christopher J
|e verfasserin
|4 aut
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|a Tuca, Emilian
|e verfasserin
|4 aut
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|a DiLabio, Gino A
|e verfasserin
|4 aut
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|a Rhodes, Larry F
|e verfasserin
|4 aut
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|i Enthalten in
|t Organometallics
|d 1998
|g 43(2024), 17 vom: 09. Sept., Seite 1904-1911
|w (DE-627)NLM098167103
|x 0276-7333
|7 nnns
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|g volume:43
|g year:2024
|g number:17
|g day:09
|g month:09
|g pages:1904-1911
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|u http://dx.doi.org/10.1021/acs.organomet.4c00263
|3 Volltext
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