Advances in Group VI Metal-Catalyzed Homogeneous Hydrogenation and Dehydrogenation Reactions

被引:10
作者
Singh, Tushar [1 ]
Atreya, Vaishnavi [1 ]
Jalwal, Sachin [1 ]
Anand, Aman [1 ]
Chakraborty, Subrata [1 ]
机构
[1] Indian Inst Technol Jodhpur, Dept Chem, Jodhpur 342037, Rajasthan, India
关键词
Base metals; Hydrogenation; dehydrogenation; sustainability; Earth-abundant; TRICARBONYL CHROMIUM COMPLEXES; TUNGSTEN NITROSYL HYDRIDES; CARBON-DIOXIDE; AMMONIA-BORANE; FORMIC-ACID; SELECTIVE HYDROGENATION; BORROWING HYDROGEN; SUBSTITUTED MOLYBDENUM; LIGAND COOPERATION; STORAGE MATERIAL;
D O I
10.1002/asia.202300758
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal-catalyzed homogeneous hydrogenation and dehydrogenation reactions for attaining plethora of organic scaffolds have evolved as a key domain of research in academia and industry. These protocols are atom-economic, greener, in line with the goal of sustainability, eventually pave the way for numerous novel environmentally benign methodologies. Appealing progress has been achieved in the realm of homogeneous catalysis utilizing noble metals. Owing to their high cost, less abundance along with toxicity issues led the scientific community to search for sustainable alternatives. In this context, earth- abundant base metals have gained substantial attention culminating enormous progress in recent years, predominantly with pincer-type complexes of nickel, cobalt, iron, and manganese. In this regard, group VI chromium, molybdenum and tungsten complexes have been overlooked and remain underdeveloped despite their earth-abundance and bio-compatibility. This review delineates a comprehensive overview in the arena of homogeneously catalysed (de)hydrogenation reactions using group VI base metals chromium, molybdenum, and tungsten till date. Various reactions have been described; hydrogenation, transfer hydrogenation, dehydrogenation, acceptorless dehydrogenative coupling, hydrogen auto transfer, along with their scope and brief mechanistic insights. Homogeneous hydrogenation and dehydrogenation reactions have emerged as atom-economic, sustainable protocols paving the way for numerous novel environmentally benign catalytic organic transformations. This review describes comprehensive overview in the area of homogeneously catalysed (de)hydrogenation reactions using earth-abundant group VI base metals chromium, molybdenum, and tungsten.+image
引用
收藏
页数:34
相关论文
共 196 条
[1]   Imines, enamines and oximes [J].
Adams, JP .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 2000, (02) :125-139
[2]   Selective ethylene oligomerization: Recent advances in chromium catalysis and mechanistic investigations [J].
Agapie, Theodor .
COORDINATION CHEMISTRY REVIEWS, 2011, 255 (7-8) :861-880
[3]   HCOOH disproportionation to MeOH promoted by molybdenum PNP complexes [J].
Alberico, Elisabetta ;
Leischner, Thomas ;
Junge, Henrik ;
Kammer, Anja ;
Sang, Rui ;
Seifert, Jenny ;
Baumann, Wolfgang ;
Spannenberg, Anke ;
Junge, Kathrin ;
Beller, Matthias .
CHEMICAL SCIENCE, 2021, 12 (39) :13101-13119
[4]   Catalytic and Organometallic Chemistry of Earth-Abundant Metals [J].
Albrecht, Martin ;
Bedford, Robin ;
Plietker, Bernd .
ORGANOMETALLICS, 2014, 33 (20) :5619-5621
[5]   First-Row Transition Metal (De)Hydrogenation Catalysis Based On Functional Pincer Ligands [J].
Alig, Lukas ;
Fritz, Maximilian ;
Schneider, Sven .
CHEMICAL REVIEWS, 2019, 119 (04) :2681-2751
[6]   Origins, current status, and future challenges of green chemistry [J].
Anastas, PT ;
Kirchhoff, MM .
ACCOUNTS OF CHEMICAL RESEARCH, 2002, 35 (09) :686-694
[7]  
Andersson P. G., 2008, MODERN REDUCTION MET
[8]   A molybdenum complex bearing PNP-type pincer ligands leads to the catalytic reduction of dinitrogen into ammonia [J].
Arashiba, Kazuya ;
Miyake, Yoshihiro ;
Nishibayashi, Yoshiaki .
NATURE CHEMISTRY, 2011, 3 (02) :120-125
[9]  
Aresta M., 2010, CARBON DIOXIDE CHEM
[10]   Catalysis for the Valorization of Exhaust Carbon: from CO2 to Chemicals, Materials, and Fuels. Technological Use of CO2 [J].
Aresta, Michele ;
Dibenedetto, Angela ;
Angelini, Antonella .
CHEMICAL REVIEWS, 2014, 114 (03) :1709-1742