Synergistic effects altering reaction pathways: The case of glucose hydrogenation over Fe-Ni catalysts

2021 ◽  
Vol 288 ◽  
pp. 119997
Author(s):  
Yang Fu ◽  
Lipeng Ding ◽  
Michael L. Singleton ◽  
Hosni Idrissi ◽  
Sophie Hermans
2019 ◽  
Vol 377 ◽  
pp. 343-357 ◽  
Author(s):  
Geun-Ho Han ◽  
Min Woo Lee ◽  
Soohyung Park ◽  
Ho Joong Kim ◽  
Jae-Pyoung Ahn ◽  
...  

Molecules ◽  
2019 ◽  
Vol 24 (2) ◽  
pp. 364 ◽  
Author(s):  
Rui Kong ◽  
Shuai-Bo Han ◽  
Jing-Ying Wei ◽  
Xiao-Chong Peng ◽  
Zhen-Biao Xie ◽  
...  

In our studies on the catalytic activity of Group IVB transition metal Lewis acids, Hf(OTf)4 was identified as a highly potent catalyst for ”one-pot, three-component” Biginelli reaction. More importantly, it was found that solvent-free conditions, in contrast to solvent-based conditions, could dramatically promote the Hf(OTf)4-catalyzed formation of 3,4-dihydro-pyrimidin-2-(1H)-ones. To provide a mechanistic explanation, we closely examined the catalytic effects of Hf(OTf)4 on all three potential reaction pathways in both “sequential bimolecular condensations” and “one-pot, three-component” manners. The experimental results showed that the synergistic effects of solvent-free conditions and Hf(OTf)4 catalysis not only drastically accelerate Biginelli reaction by enhancing the imine route and activating the enamine route but also avoid the formation of Knoevenagel adduct, which may lead to an undesired byproduct. In addition, 1H-MMR tracing of the H-D exchange reaction of methyl acetoacetate in MeOH-d4 indicated that Hf(IV) cation may significantly accelerate ketone-enol tautomerization and activate the β-ketone moiety, thereby contributing to the overall reaction rate.


Author(s):  
Hasan Masitah ◽  
Toshiki Asakoshi ◽  
Hiroki Muroyama ◽  
Toshiaki Matsui ◽  
Koichi Eguchi

Supported Ni catalysts are active in CO2 methanation. To understand the reaction mechanism is important for the development of highly-active catalysts. In this study, we investigated the reaction pathways of...


2017 ◽  
Vol 296 ◽  
pp. 144-153 ◽  
Author(s):  
Stefanie C.M. Mizuno ◽  
Adriano H. Braga ◽  
Carla E. Hori ◽  
João Batista O. Santos ◽  
José Maria C. Bueno

Author(s):  
W.W. Adams ◽  
S. J. Krause

Rigid-rod polymers such as PBO, poly(paraphenylene benzobisoxazole), Figure 1a, are now in commercial development for use as high-performance fibers and for reinforcement at the molecular level in molecular composites. Spinning of liquid crystalline polyphosphoric acid solutions of PBO, followed by washing, drying, and tension heat treatment produces fibers which have the following properties: density of 1.59 g/cm3; tensile strength of 820 kpsi; tensile modulus of 52 Mpsi; compressive strength of 50 kpsi; they are electrically insulating; they do not absorb moisture; and they are insensitive to radiation, including ultraviolet. Since the chain modulus of PBO is estimated to be 730 GPa, the high stiffness also affords the opportunity to reinforce a flexible coil polymer at the molecular level, in analogy to a chopped fiber reinforced composite. The objectives of the molecular composite concept are to eliminate the thermal expansion coefficient mismatch between the fiber and the matrix, as occurs in conventional composites, to eliminate the interface between the fiber and the matrix, and, hopefully, to obtain synergistic effects from the exceptional stiffness of the rigid-rod molecule. These expectations have been confirmed in the case of blending rigid-rod PBZT, poly(paraphenylene benzobisthiazole), Figure 1b, with stiff-chain ABPBI, poly 2,5(6) benzimidazole, Fig. 1c A film with 30% PBZT/70% ABPBI had tensile strength 190 kpsi and tensile modulus of 13 Mpsi when solution spun from a 3% methane sulfonic acid solution into a film. The modulus, as predicted by rule of mixtures, for a film with this composition and with planar isotropic orientation, should be 16 Mpsi. The experimental value is 80% of the theoretical value indicating that the concept of a molecular composite is valid.


1980 ◽  
Vol 41 (C1) ◽  
pp. C1-337-C1-337
Author(s):  
Yu. V. Maksimov ◽  
R. Arents ◽  
I. P. Suzdalev ◽  
V. K. Yatsimirski
Keyword(s):  

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