Thermal Dehydrogenation and Hydrolysis of BH3NH3 Catalyzed by Cyclic (Alkyl)(amino)carbene Iridium Complexes under Mild Conditions

Author(s):  
Lei Zhou ◽  
Dejin Zhang ◽  
Jinling Hu ◽  
Youting Wu ◽  
Jiao Geng ◽  
...  
2020 ◽  
Vol 204 ◽  
pp. 106407 ◽  
Author(s):  
Shengxin An ◽  
Wenzhi Li ◽  
Fengyang Xue ◽  
Xu Li ◽  
Ying Xia ◽  
...  

2017 ◽  
Vol 39 (4) ◽  
pp. 423 ◽  
Author(s):  
George Meredite Cunha de Castro ◽  
Norma Maria Barros Benevides ◽  
Maulori Curié Cabral ◽  
Rafael De Souza Miranda ◽  
Enéas Gomes Filho ◽  
...  

 The seaweeds are bio-resource rich in sulfated and neutral polysaccharides. The tropical seaweed species used in this study (Solieria filiformis), after dried, shows 65.8% (w/w) carbohydrate, 9.6% (w/w) protein, 1.7% (w/w) lipid, 7.0% (w/w) moisture and 15.9% (w/w) ash. The dried seaweed was easily hydrolyzed under mild conditions (0.5 M sulfuric acid, 20 min.), generating fermentable monosaccharides with a maximum hydrolysis efficiency of 63.21%. Galactose and glucose present in the hydrolyzed were simultaneously fermented by Saccharomyces cerevisiae when the yeast was acclimated to galactose and cultivated in broth containing only galactose. The kinetic parameters of the fermentation of the seaweed hydrolyzed were Y(P⁄S) = 0.48 ± 0.02 g.g−1, PP = 0.27 ± 0.04 g.L−1.h−1, h = 94.1%, representing a 41% increase in bioethanol productivity. Therefore, S. filiformis was a promising renewable resource of polysaccharides easily hydrolyzed, generating a broth rich in fermentable monosaccharides for ethanol production. 


2001 ◽  
Vol 2 (3-4) ◽  
pp. 135-138 ◽  
Author(s):  
John West ◽  
B. Peter Williams ◽  
Nicola Young ◽  
Colin Rhodes ◽  
Graham J. Hutchings

2018 ◽  
Vol 43 (14) ◽  
pp. 7038-7045 ◽  
Author(s):  
Rui Lu ◽  
Min Hu ◽  
Caili Xu ◽  
Yi Wang ◽  
Yun Zhang ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 24 (41) ◽  
pp. no-no
Author(s):  
T. BEARD ◽  
M. A. COHEN ◽  
J. S. PARRATT ◽  
N. J. TURNER ◽  
J. CROSBY ◽  
...  

2009 ◽  
Vol 64 (11-12) ◽  
pp. 1558-s1579 ◽  
Author(s):  
Christian Däschlein ◽  
Carsten Strohmann

The selective cleavage of the strong and poorly reactive Si-O-Si bond in functionalized siloxanes under mild conditions is a decisive task for modern synthetic chemistry. Simple treatment of the aminomethyl-functionalized disiloxanes 1, 6, (R,R)-7 and 8 ([R2(CH2NR')SiO]2, R =Me or Ph, NR'= NC5H10, NC5H8(CH3)2 or NC4H7(CH3)) with zinc(II) bromide and zinc(II) chloride, respectively, results in the formation of highly hydrolysis-stable, molecular zinc silanolates which were long time supposed to be unstable in the presence of water. Both, the selective cleavage of the Si-O-Si bond as well as the formation of the molecular zinc silanolates are independent of the substituents at silicon, the used zinc(II) salt or the aminomethyl side arm. Detailed structural studies showed that zwitterionic interactions are the reason for the high stability towards hydrolysis of the formed zinc silanolates 9, 10, (R,R)-11 and 12. NMR studies are indicative of the same structure of these molecular systems in solution as in the solid state


1993 ◽  
Vol 4 (6) ◽  
pp. 1085-1104 ◽  
Author(s):  
Timothy Beard ◽  
Mark A. Cohen ◽  
Julian S. Parratt ◽  
Nicholas J. Turner ◽  
John Crosby ◽  
...  

2015 ◽  
Vol 38 (6) ◽  
pp. 1127-1141 ◽  
Author(s):  
Arturo Sanchez ◽  
Juan Carlos Gil ◽  
Oscar A. Rojas-Rejón ◽  
Ana P. de Alba ◽  
Andrea Medina ◽  
...  

2008 ◽  
Vol 63 (7) ◽  
pp. 1-7
Author(s):  
Arthur H. Schmidt ◽  
Peter Müllen ◽  
Gabriele Wallmeyer ◽  
Claudia Plutniok ◽  
Peter R. Wiesert

Squaric dichloride (3) reacts with Schiff bases 5 under mild conditions to give 1 : 1 adducts 7. On recrystallisation from alcohols, these adducts are converted to the respective N-(α-alkoxybenzyl)- squaric amide chlorides 8. The reaction has been extended to perchlorocyclobutenone 4. Thus, addition products 14 have been obtained from the reaction of 4 with Schiff bases 5, which, on recrystallisation from alcohols, afforded N-(α-alkoxybenzyl)-substituted 3-amino-2,4,4-trichloro-cyclobuten- 1-ones 15. Hydrolysis of the adducts 14 gave the aminotrichlorocyclobutenones 17 in good yield.


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