scholarly journals Side Chain-Directed Assembly of Large Discotic π-Conjugated Molecules: Toward Tuning and Stabilization of Mesophases

2015 ◽  
Vol 28 (4) ◽  
pp. 583-587 ◽  
Author(s):  
Yusuke Tsutsui ◽  
Tsuneaki Sakurai ◽  
Kenichi Kato ◽  
Masaki Takata ◽  
Shu Seki
2014 ◽  
Vol 6 (10) ◽  
pp. 941-941 ◽  
Author(s):  
Martin J. Hollamby ◽  
Maciej Karny ◽  
Paul H. H. Bomans ◽  
Nico A. J. M. Sommerdijk ◽  
Akinori Saeki ◽  
...  

2014 ◽  
Vol 6 (8) ◽  
pp. 690-696 ◽  
Author(s):  
Martin J. Hollamby ◽  
Maciej Karny ◽  
Paul H. H. Bomans ◽  
Nico A. J. M. Sommerdjik ◽  
Akinori Saeki ◽  
...  

2017 ◽  
Vol 5 (8) ◽  
pp. 1935-1943 ◽  
Author(s):  
Cheng Zhang ◽  
Dafei Yuan ◽  
Hao Wu ◽  
Eliot Gann ◽  
Lars Thomsen ◽  
...  

Control of molecular ordering and packing of π-conjugated molecules in the solid state is crucial for enhancing the charge transport properties in organic electronics.


1998 ◽  
Vol 95 (6) ◽  
pp. 1351-1354 ◽  
Author(s):  
C.-M. Bouché ◽  
P. Le Barny ◽  
H. Facoetti ◽  
F. Soyer ◽  
P. Robin
Keyword(s):  

1984 ◽  
Vol 51 (03) ◽  
pp. 358-361 ◽  
Author(s):  
H Bechtold ◽  
K Andrassy ◽  
E Jähnchen ◽  
J Koderisch ◽  
H Koderisch ◽  
...  

SummaryIn 8 patients on no oral intake and with parenteral alimentation, administration of cephalosporins with N-methyl-thiotetrazole side chain (moxalactam, cefamandole), was associated with prolongation of prothrombin time, appearance in the circulation of descarboxy-prothrombin (counter immunoelectrophoresis and echis carinatus assay) and diminution of protein C. Acute administration of 10 mg vitamin Ki was followed by the transient appearance of vitamin K1 2,3-epoxide, indicating an impaired hepatocellular regeneration of vitamin K1 from the epoxide. Impaired hepatic vitamin K1 metabolism, tentatively ascribed to the N-methyl-thiotetrazole group, is one (but possibly not the only) cause of bleeding complications and depression of vitamin K1dependent procoagulants in patients treated with the new class of cephalosporins.


1961 ◽  
Vol 36 (4) ◽  
pp. 511-519 ◽  
Author(s):  
Margaret Wiener ◽  
Charles I. Lupa ◽  
E. Jürgen Plotz

ABSTRACT 17α-hydroxyprogesterone-4-14C-17α-caproate (HPC), a long-acting progestational agent, was incubated with homogenates of rat liver and human placenta. The rat liver was found to reduce Ring A of HPC under anaerobic conditions to form allopregnane-3β,17α-diol-20-one-17α-caproate and pregnane-3β,17α-diol-20-one-17α-caproate, the allopregnane isomer being the major product. The caproic acid ester was neither removed nor altered during the incubation. Placental tissue did not attack HPC under conditions where the 20-ketone of progesterone was reduced. It is postulated that this absence of attack on the side chain is due to steric hindrance from the caproate ester, and that this may account for the prolonged action of HPC.


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