N-heterocyclic bis-carbene palladium complexes derived from functionalized naphthalimides - Synthesis, Structure elucidation and DFT study
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作者:
Dangalov, Miroslav
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Bulgarian Acad Sci, Inst Organ Chem Ctr Phytochem, 9 Acad G Bonchev Str, Sofia 1113, BulgariaBulgarian Acad Sci, Inst Organ Chem Ctr Phytochem, 9 Acad G Bonchev Str, Sofia 1113, Bulgaria
Dangalov, Miroslav
[1
]
Petrov, Petar
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Sofia Univ, Dept Organ Chem, Fac Chem & Pharm, St Kliment Ohridsky,1,James Bourchier Bl, Sofia 1164, BulgariaBulgarian Acad Sci, Inst Organ Chem Ctr Phytochem, 9 Acad G Bonchev Str, Sofia 1113, Bulgaria
Petrov, Petar
[2
]
Vassilev, Nikolay G.
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Bulgarian Acad Sci, Inst Organ Chem Ctr Phytochem, 9 Acad G Bonchev Str, Sofia 1113, BulgariaBulgarian Acad Sci, Inst Organ Chem Ctr Phytochem, 9 Acad G Bonchev Str, Sofia 1113, Bulgaria
Vassilev, Nikolay G.
[1
]
机构:
[1] Bulgarian Acad Sci, Inst Organ Chem Ctr Phytochem, 9 Acad G Bonchev Str, Sofia 1113, Bulgaria
[2] Sofia Univ, Dept Organ Chem, Fac Chem & Pharm, St Kliment Ohridsky,1,James Bourchier Bl, Sofia 1164, Bulgaria
Two new bis-carbene (Pd(NHC)(2)Cl-2 and Pd(NHC)(NHC`)Br-2) complexes derived from substituted 1,8-naphthalimides were synthesized. All complexes were fully characterized by NMR spectra, which indicate trans orientation of the NHC ligands. H-1 and C-13 NMR spectra of complex Pd(NHC)(2)Cl-2 are influenced by existence of trans-syn and trans-anti rotamers. The dynamic behaviour in solution of the complex Pd(NHC)(2)Cl-2 was studied by H-1 NMR spectra in the temperature range of 293-403 K. The rotational barrier is experimentally estimated to 20 kcal/mol at 298 K. The DFT calculations reproduce the experimental data very well. The analysis of DFT calculations suggests electronic origin of the restricted rotation around Pd-C carbene bond. The electron-donating properties of reported system are situated between unsaturated and saturated five-membered ring NHC ligands. (C) 2021 Elsevier B.V. All rights reserved.