LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 4 of total 4

Search options

  1. Article ; Online: Chelating σ-Aryl Post-Metallocenes: Probing Intramolecular [C-H···F-C] Interactions and Unusual Reaction Pathways.

    Liu, Cham-Chuen / Chan, Michael C W

    Accounts of chemical research

    2015  Volume 48, Issue 6, Page(s) 1580–1590

    Abstract: Our interest in chelating σ-aryl ancillary ligands was motivated by their potential to impart unusual reactivity, since we envisioned that σ-donors with minimal π-donation would create a catalytic center with enhanced electrophilicity. We developed a ... ...

    Abstract Our interest in chelating σ-aryl ancillary ligands was motivated by their potential to impart unusual reactivity, since we envisioned that σ-donors with minimal π-donation would create a catalytic center with enhanced electrophilicity. We developed a family of Group 4 post-metallocene catalysts supported by pyridine-2-phenolate-6-(σ-aryl) [O,N,C] ligands bearing a fluorinated moiety in the vicinity of the metal. Notable features of these meta-substituted tris(hetero)aryl frameworks include their coordination geometry and inherent rigidity. For the first time, the elusive C-H···F-C interaction was manifested as NMR-discernible (1)H-(19)F coupling in solution and characterized by a neutron diffraction study. Their existence carries implications for catalyst design and in the context of weak attractive ligand-polymer interactions (WALPI), since they substantiate the practical viability of the ortho-F···H(β) ligand-polymer interactions proposed for living Group 4 fluorinated bis(phenoxyimine) catalysts. In metal-catalyzed olefin polymerization reactions, the notion of noncovalent interactions between an active ancillary ligand and the growing polymer chain is new. These interactions must be fragile and transient in nature, otherwise the intrinsic chain propagation process would be disrupted, and inherently tunable attractive forces such as hydrogen bonds are ideally suited to this role. The nature, relevance, and usability of extremely weak hydrogen bonds such as C-H···F-C has been a topical yet controversial area of research. We subsequently prepared a series of Group 4 complexes supported by fluorinated (σ-aryl)-2-phenolate-6-pyridyl [O,C,N] ligands. [(1)H,(19)F]-HMBC NMR experiments were conducted to probe the observed (1)H-(19)F coupling, and specifically separate contributions from scalar (J) coupling and cross-correlation (CR) interference. For the first time, a significant scalar component was confirmed for the (1)H-(19)F coupling in Ti-[O,C,N] and [O,N,C] complexes, which occurs with chemical connectivity across intramolecular C-H···F-C interactions. This result is important because the applicability of weak attractive ligand-polymer interactions in catalysis is feasible only if the observed coupling and hence the noncovalent interaction is genuine. The verified intramolecular C-H···F-C contacts in these complexes can therefore be considered as synthetic models for ligand-polymer interactions in olefin polymerization processes. Significantly, reports concerning late transition metal systems have appeared that hint at the generality of the WALPI concept for modulating polymerization reactions. We evaluated the olefin polymerization reactivity of Ti-[O,N,C] catalysts through judicious substitution. DFT calculations, which revealed diverse kinetically competitive reaction pathways and active sites (including unusual ethylene-assimilated species) in addition to normal chain propagation, were also employed to rationalize polymerization efficiencies. Further developments in catalytic applications of multidentate σ-aryl ligand systems and novel reactivity of the corresponding complexes can be envisaged.
    MeSH term(s) Alkenes/chemical synthesis ; Alkenes/chemistry ; Chelating Agents/chemical synthesis ; Chelating Agents/chemistry ; Molecular Conformation ; Organometallic Compounds/chemical synthesis ; Organometallic Compounds/chemistry ; Quantum Theory
    Chemical Substances Alkenes ; Chelating Agents ; Organometallic Compounds
    Language English
    Publishing date 2015-06-16
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1483291-4
    ISSN 1520-4898 ; 0001-4842
    ISSN (online) 1520-4898
    ISSN 0001-4842
    DOI 10.1021/acs.accounts.5b00008
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Multifaceted chelating μ-(η(3):η(3)-antifacial)-(cis-C4R2H2) coordination motif in binuclear complexes.

    Liu, Cham-Chuen / Chan, Michael C W / Lo, Po-Kam / Lau, Kai-Chung / Yiu, Shek-Man

    Chemical communications (Cambridge, England)

    2016  Volume 52, Issue 74, Page(s) 11056–11059

    Abstract: A novel μ-C4R2H2 core structure (formed by an unprecedented regioselective, redox-neutral C(sp(2))-C(sp(2)) coupling process) in binuclear group 4 complexes displays adaptable coordination and accommodates different metal sizes, and is sufficiently ... ...

    Abstract A novel μ-C4R2H2 core structure (formed by an unprecedented regioselective, redox-neutral C(sp(2))-C(sp(2)) coupling process) in binuclear group 4 complexes displays adaptable coordination and accommodates different metal sizes, and is sufficiently robust to promote interesting catalytic reactivity at the bimetallic centers.
    Language English
    Publishing date 2016-09-25
    Publishing country England
    Document type Journal Article
    ZDB-ID 1472881-3
    ISSN 1364-548X ; 1359-7345 ; 0009-241X
    ISSN (online) 1364-548X
    ISSN 1359-7345 ; 0009-241X
    DOI 10.1039/c6cc05535d
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article: Multifaceted chelating μ-(η3:η3-antifacial)-(cis-C4R2H2) coordination motif in binuclear complexes

    Liu, Cham-Chuen / Chan, Michael C. W / Lo, Po-Kam / Lau, Kai-Chung / Yiu, Shek-Man

    Chemical communications. 2016 Sept. 8, v. 52, no. 74

    2016  

    Abstract: A novel μ-C4R2H2 core structure (formed by an unprecedented regioselective, redox-neutral C(sp2)–C(sp2) coupling process) in binuclear group 4 complexes displays adaptable coordination and accommodates different metal sizes, and is sufficiently robust to ...

    Abstract A novel μ-C4R2H2 core structure (formed by an unprecedented regioselective, redox-neutral C(sp2)–C(sp2) coupling process) in binuclear group 4 complexes displays adaptable coordination and accommodates different metal sizes, and is sufficiently robust to promote interesting catalytic reactivity at the bimetallic centers.
    Keywords chemical compounds ; chemical reactions ; regioselectivity
    Language English
    Dates of publication 2016-0908
    Size p. 11056-11059.
    Publishing place The Royal Society of Chemistry
    Document type Article
    ZDB-ID 1472881-3
    ISSN 1364-548X ; 1359-7345 ; 0009-241X
    ISSN (online) 1364-548X
    ISSN 1359-7345 ; 0009-241X
    DOI 10.1039/c6cc05535d
    Database NAL-Catalogue (AGRICOLA)

    More links

    Kategorien

  4. Article ; Online: Scalar coupling across [C-H···F-C] interactions in (σ-aryl)-chelating post-metallocenes.

    So, Loi-Chi / Liu, Cham-Chuen / Chan, Michael C W / Lo, Jerry C Y / Sze, Kong-Hung / Zhu, Nianyong

    Chemistry (Weinheim an der Bergstrasse, Germany)

    2012  Volume 18, Issue 2, Page(s) 565–573

    Abstract: The nature and importance of C-H···F-C interactions is a topical yet controversial issue, and the development of spectroscopic methods to probe such contacts is therefore warranted. A series of Group 4 bis(benzyl) complexes supported by (σ-aryl)-2- ... ...

    Abstract The nature and importance of C-H···F-C interactions is a topical yet controversial issue, and the development of spectroscopic methods to probe such contacts is therefore warranted. A series of Group 4 bis(benzyl) complexes supported by (σ-aryl)-2-phenolate-6-pyridyl [O,C,N-R(1)] ligands bearing a fluorinated R(1) group (CF(3) or F) in the vicinity of the metal has been prepared. The X-ray crystal structure of the CF(3)-substituted Hf derivative features intramolecular C-H···F-C and Hf···F-C contacts. All complexes have been characterized by multinuclear NMR spectroscopy. The (1)H and (13)C NMR spectra of [M(O,C,N-CF(3))(CH(2)Ph)(2)] derivatives display coupling (assigned to (1h)J(HF) and (2h)J(CF) for Ti; (3)J(HF) and (2)J(CF) (through M···F) for Hf and Zr) between the benzyl CH(2) and CF(3) moieties. [(1)H,(19)F]-HMBC NMR experiments have been performed for the M-[O,C,N-R(1)] complexes and their [O,N,C] counterparts, revealing significant scalar coupling across the C-H···F-C interactions for Ti-[O,C,N] and [O,N,C] species.
    MeSH term(s) Carbon/chemistry ; Chelating Agents/chemistry ; Crystallography, X-Ray ; Fluorine/chemistry ; Hydrogen Bonding ; Ligands ; Models, Molecular ; Organometallic Compounds/chemistry
    Chemical Substances Chelating Agents ; Ligands ; Organometallic Compounds ; metallocene ; Fluorine (284SYP0193) ; Carbon (7440-44-0)
    Language English
    Publishing date 2012-01-09
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1478547-x
    ISSN 1521-3765 ; 0947-6539
    ISSN (online) 1521-3765
    ISSN 0947-6539
    DOI 10.1002/chem.201102439
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top