Dhara Debabrata, Das Shubhajit, Pati Swapan K, Scheschkewitz David, Chandrasekhar Vadapalli, Jana Anukul
Tata Institute of Fundamental Research Hyderabad, Gopanpally, Hyderabad-, 500107, Telangana, India.
Theoretical Sciences Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore-, 560064, India.
Angew Chem Int Ed Engl. 2019 Oct 21;58(43):15367-15371. doi: 10.1002/anie.201909798. Epub 2019 Sep 12.
An NHC-coordinated diphosphene is employed as ligand for the synthesis of a hydrocarbon-soluble monomeric Au hydride, which readily adds CO at room temperature yielding the corresponding Au formate. The reversible reaction can be expedited by the addition of NHC, which induces β-hydride shift and the removal of CO from equilibrium through the formation of an NHC-CO adduct. The Au formate is alternatively formed by dehydrogenative coupling of the Au hydride with formic acid (HCO H), thus in total establishing a reaction sequence for the Au hydride mediated dehydrogenation of HCO H as chemical hydrogen storage material.
一种由氮杂环卡宾(NHC)配位的双膦烯被用作配体,用于合成一种可溶于烃类的单体氢化金,该氢化金在室温下能迅速与一氧化碳(CO)反应生成相应的甲酸金。通过添加氮杂环卡宾可以加速该可逆反应,氮杂环卡宾会引发β-氢化物转移,并通过形成氮杂环卡宾-CO加合物使平衡中的CO被除去。甲酸金也可以通过氢化金与甲酸(HCOOH)的脱氢偶联反应形成,从而总共建立了一个以氢化金介导的甲酸作为化学储氢材料的脱氢反应序列。