메뉴 건너뛰기




Volumn 21, Issue 40, 2015, Pages 13904-13908

How and Why Does Ni0 Promote Smooth Etheric C-O Bond Cleavage and C-C Bond Formation? A Theoretical Study

Author keywords

aryl alkyl ether; cross coupling; DFT calculations; nickel; reaction mechanism

Indexed keywords

CATALYSIS; CATALYSTS; CHEMICAL ACTIVATION; DENSITY FUNCTIONAL THEORY; ETHERS; NICKEL; TRANSITION METALS;

EID: 84941809041     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201502114     Document Type: Article
Times cited : (73)

References (85)
  • 1
    • 84941804556 scopus 로고    scopus 로고
    • Reviews on TM-catalyzed cross-coupling by using phenol derivatives
    • Reviews on TM-catalyzed cross-coupling by using phenol derivatives:
  • 10
    • 14744304154 scopus 로고    scopus 로고
    • Angew. Chem. 2004, 116, 2482;
    • (2004) Angew. Chem. , vol.116 , pp. 2482
  • 21
    • 57749094839 scopus 로고    scopus 로고
    • Angew. Chem. 2008, 120, 4944;
    • (2008) Angew. Chem. , vol.120 , pp. 4944
  • 27
    • 84954402539 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 13126;
    • (2014) Angew. Chem. , vol.126 , pp. 13126
  • 42
    • 0032496954 scopus 로고    scopus 로고
    • special cases, such as pincer structures, direct oxidative additions under mild conditions could proceed, see:, Also see ref. [7d].
    • In special cases, such as pincer structures, direct oxidative additions under mild conditions could proceed, see:, M. E. van der Boom, S.-Y. Liou, Y. Ben-David, L. J. W. Shimon, D. Milstein, J. Am. Chem. Soc. 1998, 120, 6531. Also see ref. [7d].
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 6531
    • Van Der Boom, M.E.1    Liou, S.-Y.2    Ben-David, Y.3    Shimon, L.J.W.4    Milstein, D.5
  • 54
    • 84941801894 scopus 로고    scopus 로고
    • 2O.
    • 2O.
  • 55
    • 85073174178 scopus 로고    scopus 로고
    • 3, imidazole (NHC), and some pincer-type ligands are also effective for these reactions. Computational investigations on the effects of different ligands are in progress.
    • 3, imidazole (NHC), and some pincer-type ligands are also effective for these reactions. Computational investigations on the effects of different ligands are in progress.
  • 58
    • 84941805641 scopus 로고    scopus 로고
    • Complexes, such as CP1 or CPa, are usually regarded as the starting point for calculation (see ref. [7e], [8]), since such Ni-arene complexes have been extensively studied theoretically and experimentally. For theoretical studies on the formation process, see
    • Complexes, such as CP1 or CPa, are usually regarded as the starting point for calculation (see ref. [7e], [8]), since such Ni-arene complexes have been extensively studied theoretically and experimentally. For theoretical studies on the formation process, see:
  • 61
    • 50549093469 scopus 로고    scopus 로고
    • Also see: ref. [8c]; for representative reports on the isolation of such complexes, see
    • T. A. Ateşin, T. Li, S. Lachaize, J. J. García, W. D. Jones, Organometallics 2008, 27, 3811; Also see: ref. [8c]; for representative reports on the isolation of such complexes, see:
    • (2008) Organometallics , vol.27 , pp. 3811
    • Ateşin, T.A.1    Li, T.2    Lachaize, S.3    García, J.J.4    Jones, W.D.5
  • 63
    • 78649241656 scopus 로고    scopus 로고
    • 3 to save calculation time/resource). The reaction pathway and energy profiles are essentially the same as those reported (see the Supporting Information).
    • 3 to save calculation time/resource). The reaction pathway and energy profiles are essentially the same as those reported (see the Supporting Information).
    • (2010) Organometallics , vol.29 , pp. 6077
    • Hatnean, J.A.1    Beck, R.2    Borrelli, J.D.3    Johnson, S.A.4
  • 69
    • 84941802366 scopus 로고    scopus 로고
    • 0 compounds with alkyl anion is known as the "nickel effect". For a critical review, see
    • 0 compounds with alkyl anion is known as the "nickel effect". For a critical review, see:
  • 71
    • 0001285755 scopus 로고
    • for representative examples, see
    • Angew. Chem. 1988, 100, 189; for representative examples, see:
    • (1988) Angew. Chem. , vol.100 , pp. 189
  • 73
    • 84985723178 scopus 로고
    • 2] (tmeda=tetramethylethylendiamine) and obtained a geometry (data not shown) that was essentially the same as the reported single-crystal structure
    • 2] (tmeda=tetramethylethylendiamine) and obtained a geometry (data not shown) that was essentially the same as the reported single-crystal structure:, W. Kaschube, K.-R. Pörschke, K. Angermund, C. Krüger, G. Wilke, Chem. Ber. 1988, 121, 1921;
    • (1988) Chem. Ber. , vol.121 , pp. 1921
    • Kaschube, W.1    Pörschke, K.-R.2    Angermund, K.3    Krüger, C.4    Wilke, G.5
  • 75
    • 84926655247 scopus 로고    scopus 로고
    • Angew. Chem. 2015, 127, 1603.
    • (2015) Angew. Chem. , vol.127 , pp. 1603
  • 76
    • 84941806491 scopus 로고    scopus 로고
    • Recent examples for coupling reactions involving Ni-ate complex
    • Recent examples for coupling reactions involving Ni-ate complex:
  • 79
    • 79551472329 scopus 로고    scopus 로고
    • Angew. Chem. 2010, 122, 4670;
    • (2010) Angew. Chem. , vol.122 , pp. 4670
  • 81
  • 82
    • 84877049847 scopus 로고    scopus 로고
    • 2 is calculated according to the reported way, see:, Note that location of suitable aggregation state for organometallics is very important for determining the correct energy change in calculation, for recent examples, see
    • 2 is calculated according to the reported way, see:, G. Jiménez-Osés, A. J. Brockway, J. T. Shaw, K. N. Houk, J. Am. Chem. Soc. 2013, 135, 6633. Note that location of suitable aggregation state for organometallics is very important for determining the correct energy change in calculation, for recent examples, see:
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 6633
    • Jiménez-Osés, G.1    Brockway, A.J.2    Shaw, J.T.3    Houk, K.N.4
  • 85
    • 84921333622 scopus 로고    scopus 로고
    • 0 (M=Ni and Pd) and π-ligand (arene, ethylene, etc.) has been well studied by several groups: see refs. [8b], [8c], and [22a], also see:, Our results are in good agreement with their conclusions, i.e., the Pd complexes are less stable than the Ni complexes, mainly due to weaker d-π∗ back-donation. We also recalculated two representative examples from Nakamura's work (ref. [18b]). The result was consistent with our present findings, see the Supporting Information.
    • 0 (M=Ni and Pd) and π-ligand (arene, ethylene, etc.) has been well studied by several groups: see refs. [8b], [8c], and [22a], also see:, F. Hering, J. Nitsch, U. Paul, A. Steffen, F. M. Bickelhaupt, U. Radius, Chem. Sci. 2015, 6, 1426. Our results are in good agreement with their conclusions, i.e., the Pd complexes are less stable than the Ni complexes, mainly due to weaker d-π∗ back-donation. We also recalculated two representative examples from Nakamura's work (ref. [18b]). The result was consistent with our present findings, see the Supporting Information.
    • (2015) Chem. Sci. , vol.6 , pp. 1426
    • Hering, F.1    Nitsch, J.2    Paul, U.3    Steffen, A.4    Bickelhaupt, F.M.5    Radius, U.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.