Synthesis and coordination of hybrid phosphinoferrocenes with extended donor pendants
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F22%3A10452537" target="_blank" >RIV/00216208:11310/22:10452537 - isvavai.cz</a>
Result on the web
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=J0O6.ViTo0" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=J0O6.ViTo0</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/d2dt02514k" target="_blank" >10.1039/d2dt02514k</a>
Alternative languages
Result language
angličtina
Original language name
Synthesis and coordination of hybrid phosphinoferrocenes with extended donor pendants
Original language description
Combining a phosphinoferrocene fragment with extended muItidonor moieties affords novel, flexible muftidonor pro-ligands. This contribution describes the synthesis of two structurally similar functional phosphines, Ph2PfcNHC(O)CH2PPh2 (1) and Ph2PfcNHCH2CH2PPh2 (2, fc = ferrocene-1,1'-diyl), and their coordination behaviour towards Pd(II). The former amidophosphine reacts with [PdCl2(MeCN)2] to produce the cheIate complex [PdCl2(1-κ(2)P,P')] as a mixture of cis and trans isomers, which convert into bis-cheIate [PdCl2(Ph2PfcNC(O)CH2PPh2-κ(3)P,P',N)] upon reacting with a strong base (KOt-Bu). In contrast, the more flexible and more basic phosphinoamine 2 directly forms the cationic bis-cheIate complex [PdCl(2-κ(3)P,P',N)]CI via spontaneous self-ionisation. Subsequent halogen abstraction with Ag[SbF6] results either in counter ion exchange to give [PdCl(2-κ(3)Fe,P',P')][SbF6] or in the formation of a structurally unique complex [PdCl(2-κ(4)Fe,P,P', N)][SbF6](2) with an Fe -> Pd dative interaction, depending on the amount of silver(I) salt used (1 or 2 equiv.).
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10402 - Inorganic and nuclear chemistry
Result continuities
Project
<a href="/en/project/GA19-09334S" target="_blank" >GA19-09334S: Uncoventional ferrocene phosphines</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Dalton Transactions
ISSN
1477-9226
e-ISSN
1477-9234
Volume of the periodical
51
Issue of the periodical within the volume
38
Country of publishing house
GB - UNITED KINGDOM
Number of pages
12
Pages from-to
14618-14629
UT code for WoS article
000851574600001
EID of the result in the Scopus database
2-s2.0-85139571828