Comptes Rendus Chimie

Vitesh Mistry

Vihar P. Georgiev

John E. McGrady

Electron transport through molecular wires based on a face-shared bioctahedral motif

Hassan Moghanian

Meisam Shabanian

Hadi Jafari

Microwave-assisted efficient synthesis of azlactone derivatives using TsCl/DMF under solvent-free conditions

Nicole Chezeau

De Réaumur à la Première Guerre Mondiale : les étapes de la maîtrise de l’acier, l’essor des aciers spéciaux

Siham Benadji

Pierre Eloy

Alexandre Léonard

Bao-Lian Su

Chérifa Rabia

Eric M. Gaigneaux

Préparation, caractérisation et réactivité de l’acide 1-vanado-11-molybdo-phosphorique supporté sur des matériaux silicatés mésoporeux dans l’oxydation du propène

Davinder Prasad

Amreeta Preetam

Mahendra Nath

Microwave-assisted green synthesis of dibenzo[a,j]xanthenes using p-dodecylbenzenesulfonic acid as an efficient Bronsted acid catalyst under solvent-free conditions

Davinder Prasad, Amreeta Preetam and Mahendra Nath*

Department of Chemistry, University of Delhi, Delhi 110 007, India

*E-mail: mnath@chemistry.du.ac.in (M. Nath)






Figure 1. 1H NMR of compound 3a.




Figure 2. 13C NMR of compound 3a.




Figure 3. 1H NMR of compound 3b.




Figure 4. 13C NMR of compound 3b.




Figure 5. 1H NMR of compound 3c.



Figure 6. 13C NMR of compound 3c.




Figure 7. 1H NMR of compound 3d.



Figure 8. 13C NMR of compound 3d.



Figure 9. 1H NMR of compound 3e.



Figure 10. 13C NMR of compound 3e.



Figure 11. 1H NMR of compound 3f.



Figure 12. 13C NMR of compound 3f.




Figure 13. 1H NMR of compound 3g.




Figure 14. 13C NMR of compound 3g.




Figure 15. 1H NMR of compound 3h.




Figure 16. 13C NMR of compound 3h.



Figure 17. 1H NMR of compound 3i.




Figure 18. 1H NMR of compound 3j.




Figure 19. 13C NMR of compound 3j.



Figure 20. 1H NMR of compound 3k.



Figure 21. 13C NMR of compound 3k.



Figure 22. 1H NMR of compound 3l.




Figure 23. 13C NMR of compound 3l.



Figure 24. 1H NMR of compound 3m.




Figure 25. 13C NMR of compound 3m.



Figure 26. 13C, DEPT-45 and DEPT-135 spectra of compound 3m.



Figure 27. COSY spectrum of compound 3m.





7





Microwave-assisted green synthesis of dibenzo[a,j]xanthenes using p-dodecylbenzenesulfonic acid as an efficient Bronsted acid catalyst under solvent-free conditions

Omar Bouaziz

Fairouz Abboub

Nawal Bayou-Khier

Mokhtar Fodili

Pascal Hoffmann

Mohamed Amari

Réactivité de l’acide déhydroacétique hydrogené en c5-c6 : obtention des pyrano-1,5-benzodiazépines différemment substituées et de la structure enaminone

Gheorghita Mitran

Éva Makó

Ákos Rédey

Ioan-Cezar Marcu

SUPPLEMENTARY MATERIAL 
 
Esterification of acetic acid with n-butanol using vanadium 
oxides supported on γ-alumina 
Estérification de l’acide acétique avec le n-butanol en présence d’oxydes de 
vanadium supportés sur γ-alumine 
 
Gheorghita Mitrana • Éva Makób • Ákos Rédeyc • Ioan-Cezar Marcua,* 
 
a Laboratory of Chemical Technology and Catalysis, Department of Organic Chemistry, Biochemistry 
& Catalysis, Faculty of Chemistry, University of Bucharest, 4-12, Blv. Regina Elisabeta, 030018 
Bucharest, Romania 
 b Institute of Materials Engineering, Faculty of Engineering, University of Pannonia, 10 Egyetem St, 
8201 Veszprém, Hungary 
c Department of Environmental Engineering and Chemical Technology, Faculty of Engineering, 
University of Pannonia, 10 Egyetem St, 8201 Veszprém, Hungary 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
                                                 
* Corresponding author. E-mail addresses: ioancezar.marcu@g.unibuc.ro ; ioancezar_marcu@yahoo.com 
Fig. S1. SEM micrographs of the vanadium-containing samples before and after the catalytic test: (a) – 
fresh 5V-Al2O3; (b) – used 5V-Al2O3; (c) – fresh 10V-Al2O3; (d) – used 10V-Al2O3. 
  
ba 
 
  
c d
 
 


Esterification of acetic acid with n-Butanol using vanadium oxides supported on γ-alumina

Agata Steenackers

Aurélie Cazet

Marie Bobowski

Yoann Rombouts

Jonathan Lefebvre

Yann Guérardel

David Tulasne

Xuefen Le Bourhis

Philippe Delannoy

Expression of GD3 synthase modifies ganglioside profile and increases migration of MCF-7 breast cancer cells

Laurent Latxague

Marie-José Dalila

Amit Patwa

Sophia Ziane

Olivier Chassande

Guilhem Godeau

Philippe Barthélémy

Glycoside nucleoside lipids (GNLs): An intrusion into the glycolipids’ world?

Axel Buchholz

Abiodun O. Eseola

Winfried Plass

Supporting Information for
Slow magnetic relaxation in mononuclear
tetrahedral cobalt(II) complexes with
2-(1H-imidazol-2-yl)phenol based ligands
Axel Buchholz,a Abiodun O. Eseola,b and Winfried Plassa,∗
a Lehrstuhl für Anorganische Chemie II, Institut für Anorganische und Analytische
Chemie, Friedrich-Schiller-Universität Jena, Humboldtstr. 8, 07743 Jena, Germany
b Department of Chemical Sciences, Redeemers University, Redemption City, Ogun
State, Nigeria
∗ sekr.plass@uni-jena.de
S1
0 1 2 3 4 5
0,0
0,5
1,0
1,5
2,0
 2.0 K
 2.5 K
 3.0 K
 3.5 K
 4.0 K
 4.5 K
M
m
ol
 [N
A
B
]
H [T]
0 1 2 3 4 5
0,0
0,5
1,0
1,5
2,0
 2.0 K
 2.5 K
 3.0 K
 3.5 K
 4.0 K
 4.5 K
 5.0 K
M
m
ol
 [N
A
B
]
H [T]
0 1 2 3 4 5
0,0
0,5
1,0
1,5
2,0
 2.0 K
 2.5 K
 3.0 K
 3.5 K
 4.0 K
 4.5 K
 5.0 K
M
m
ol
 [N
A
B
]
H [T]
Figure S1: Magnetization vs. H plots at different temperatures for the complexes
[Co(L1)2] (1) (top), [Co(L
2)2] (2) (middle), and [Co(L
3)2] (3) (bottom); lines repre-
sent the simulated values from the best fit parameters (see text); data at 2 K were
not used in the fit procedure.
S2
0 5 10 15 20 25
0,0
0,5
1,0
1,5
2,0
 2.0 K
 2.5 K
 3.0 K
 3.5 K
 4.0 K
 4.5 K
M
m
ol
 [N
A
B
]
B/T [T 10/K]
0 5 10 15 20 25
0,0
0,5
1,0
1,5
2,0
 2.0 K
 2.5 K
 3.0 K
 3.5 K
 4.0 K
 4.5 K
 5.0 K
M
m
ol
 [N
A
B
]
B/T [T 10/K]
0 5 10 15 20 25
0,0
0,5
1,0
1,5
2,0
 2.0 K
 2.5 K
 3.0 K
 3.5 K
 4.0 K
 4.5 K
 5.0 K
M
m
ol
 [N
A
B
]
B/T [T 10/K]
Figure S2: Magnetization vs. B/T plots at different temperatures for the complexes
[Co(L1)2] (1) (top), [Co(L
2)2] (2) (middle), and [Co(L
3)2] (3) (bottom); lines repre-
sent the simulated values from the best fit parameters (see text); data at 2 K were
not used in the fit procedure.
S3
2 3 4 5 6 7 8 9 10
0,1
0,2
0,3
0,4
 10 Hz
 82 Hz
 181 Hz
 306 Hz
 518 Hz
 1143 Hz
' M
 [e
m
u/
m
ol
]
T [K]
2 3 4 5 6 7 8 9
0,2
0,4
0,6
0,8
 10 Hz
 82 Hz
 181 Hz
 306 Hz
 518 Hz
' M
 [e
m
u/
m
ol
]
T [K]
2 3 4 5 6 7 8 9 10
0,2
0,4
0,6
0,8
 10 Hz
 82 Hz
 181 Hz
 306 Hz
 518 Hz
 1143 Hz
' M
 [e
m
u/
m
ol
]
T [K]
Figure S3: Temperature dependence of the in-phase χ′ ac susceptibility for the
complexes [Co(L1)2] (1) (top), [Co(L
2)2] (2) (middle), and [Co(L
3)2] (3) (bottom)
at different frequencies with an applied dc field of 400 Oe; lines are guides for the
eye.
S4


Slow magnetic relaxation in mononuclear tetrahedral cobalt(II) complexes with 2-(1H-imidazol-2-yl)phenol based ligands

Not a member yet

Electron transport through molecular wires based on a face-shared bioctahedral motif

Microwave-assisted efficient synthesis of azlactone derivatives using TsCl/DMF under solvent-free conditions

De Réaumur à la Première Guerre Mondiale : les étapes de la maîtrise de l’acier, l’essor des aciers spéciaux

Préparation, caractérisation et réactivité de l’acide 1-vanado-11-molybdo-phosphorique supporté sur des matériaux silicatés mésoporeux dans l’oxydation du propène

Microwave-assisted green synthesis of dibenzo[<i>a</i>,<i>j</i>]xanthenes using <i>p</i>-dodecylbenzenesulfonic acid as an efficient Bronsted acid catalyst under solvent-free conditions

Réactivité de l’acide déhydroacétique hydrogené en c<sub>5</sub>-c<sub>6</sub> : obtention des pyrano-1,5-benzodiazépines différemment substituées et de la structure enaminone

Esterification of acetic acid with <i>n</i>-Butanol using vanadium oxides supported on γ-alumina

Expression of G<sub>D3</sub> synthase modifies ganglioside profile and increases migration of MCF-7 breast cancer cells

Glycoside nucleoside lipids (GNLs): An intrusion into the glycolipids’ world?

Slow magnetic relaxation in mononuclear tetrahedral cobalt(II) complexes with 2-(1H-imidazol-2-yl)phenol based ligands

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