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Metal-Mediated Addition of N-Nucleophiles to Isocyanides : Mechanistic Aspects. / Kuznetsov, Maxim L.; Kukushkin, Vadim Yu.
в: Molecules (Basel, Switzerland), Том 22, № 7, 08.07.2017.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Metal-Mediated Addition of N-Nucleophiles to Isocyanides
T2 - Mechanistic Aspects
AU - Kuznetsov, Maxim L.
AU - Kukushkin, Vadim Yu
PY - 2017/7/8
Y1 - 2017/7/8
N2 - Despite the long history of the investigation of nucleophilic addition to metal-bound isocyanides, some important aspects of the reaction mechanism remain unclear even for the simplest systems. In this work, the addition of the sp³-N, sp²-N, and mixed sp²/sp³-N nucleophiles (i.e., HNMe₂, HN=CPh₂, and H₂N-N=CPh₂, respectively) to isocyanides C≡NR coordinated to the platinum(II) centers in the complexes cis-[Pt(C≡NCy)(2-pyz)(dppe)]⁺ (2-pyz = 2-pyrazyl, dmpe = Me₂PCH₂CH₂PMe₂) and cis-[PtCl₂(C≡NXyl)(C≡NMe)] was studied in detail by theoretical (DFT) methods. The mechanism of these reactions is stepwise associative rather than concerted and it includes the addition of a nucleophile to the isocyanide C atom, deprotonation of the nucleophilic moiety in the resulting intermediate, and protonation of the isocyanide N atom to give the final product. The calculated activation energy (ΔG≠) of all reactions is in the range of 19.8-22.4 kcal/mol.
AB - Despite the long history of the investigation of nucleophilic addition to metal-bound isocyanides, some important aspects of the reaction mechanism remain unclear even for the simplest systems. In this work, the addition of the sp³-N, sp²-N, and mixed sp²/sp³-N nucleophiles (i.e., HNMe₂, HN=CPh₂, and H₂N-N=CPh₂, respectively) to isocyanides C≡NR coordinated to the platinum(II) centers in the complexes cis-[Pt(C≡NCy)(2-pyz)(dppe)]⁺ (2-pyz = 2-pyrazyl, dmpe = Me₂PCH₂CH₂PMe₂) and cis-[PtCl₂(C≡NXyl)(C≡NMe)] was studied in detail by theoretical (DFT) methods. The mechanism of these reactions is stepwise associative rather than concerted and it includes the addition of a nucleophile to the isocyanide C atom, deprotonation of the nucleophilic moiety in the resulting intermediate, and protonation of the isocyanide N atom to give the final product. The calculated activation energy (ΔG≠) of all reactions is in the range of 19.8-22.4 kcal/mol.
KW - activation of small molecules
KW - carbenes
KW - DFT calculations
KW - isocyanides
KW - nitriles
KW - nucleophilic addition
KW - reaction mechanism
UR - http://www.scopus.com/inward/record.url?scp=85045039785&partnerID=8YFLogxK
U2 - 10.3390/molecules22071141
DO - 10.3390/molecules22071141
M3 - Article
C2 - 28698454
AN - SCOPUS:85045039785
VL - 22
JO - Molecules
JF - Molecules
SN - 1420-3049
IS - 7
ER -
ID: 41787337