TY - JOUR
T1 - Catalytic nitrogen fixation via direct cleavage of nitrogen-nitrogen triple bond of molecular dinitrogen under ambient reaction conditions
AU - Arashiba, Kazuya
AU - Eizawa, Aya
AU - Tanaka, Hiromasa
AU - Nakajima, Kazunari
AU - Yoshizawa, Kazunari
AU - Nishibayashi, Yoshiaki
N1 - Publisher Copyright:
© 2017 The Chemical Society of Japan.
PY - 2017
Y1 - 2017
N2 - We have now found that molybdenumiodide complexes bearing a PNP-pincer ligand have a higher catalytic activity than the so far reported molybdenumdinitrogen complexes for ammonia formation from nitrogen gas under ambient reaction conditions, up to 830 equiv being produced based on a dinitrogen-bridged dimolybdenum complex (415 equiv of ammonia based on the molybdenum atom). This remarkable catalytic activity is induced by a novel reaction pathway, where the generation of a dinitrogen-bridged dimolybdenumiodide complex is a key point to promote direct cleavage of the nitrogennitrogen triple bond of the bridging dinitrogen ligand in the MoN τNMo core.
AB - We have now found that molybdenumiodide complexes bearing a PNP-pincer ligand have a higher catalytic activity than the so far reported molybdenumdinitrogen complexes for ammonia formation from nitrogen gas under ambient reaction conditions, up to 830 equiv being produced based on a dinitrogen-bridged dimolybdenum complex (415 equiv of ammonia based on the molybdenum atom). This remarkable catalytic activity is induced by a novel reaction pathway, where the generation of a dinitrogen-bridged dimolybdenumiodide complex is a key point to promote direct cleavage of the nitrogennitrogen triple bond of the bridging dinitrogen ligand in the MoN τNMo core.
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U2 - 10.1246/bcsj.20170197
DO - 10.1246/bcsj.20170197
M3 - Article
AN - SCOPUS:85030616934
SN - 0009-2673
VL - 90
SP - 1111
EP - 1118
JO - Bulletin of the Chemical Society of Japan
JF - Bulletin of the Chemical Society of Japan
IS - 10
ER -