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1,4-Benzenedicarboximidamide, hydrochloride (1:2), polymer with thieno[3,2-b]thiophene-2,5-dicarboxaldehyde
1,4-Benzenedicarboximidamide, hydrochloride (1:2), polymer with thieno[3,2-b]thiophene-2,5-dicarboxaldehyde
CAS:2600457-34-7 M.F.:C8H4O2S2.C8H10N4.2[HCl] M.W.:431.35984
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Product: CTF-HUST-S5
Synonyms:1,4-Benzenedicarboximidamide, hydrochloride (1:2), polymer with thieno[3,2-b]thiophene-2,5-dicarboxaldehyde
CAS:2600457-34-7

Basic Information
Unit MF. C8H4O2S2.C8H10N4.2[HCl] Unit MW. 431.35984
Coordination  Metal None Linkers

1,4-Benzenedicarboximidamide, hydrochloride (1:2);
thieno[3,2-b]thiophene-2,5-dicarboxaldehyde

Pore Size 1.2 - 1.8 nm Pore Volume 0.57 cm3/g
Surface Area 454 m2/g
Analog Structure /
Product Property
Appearance Brown Red Powders  
Particle Size Nanosheet morphology, lateral size 1 - 5 μm, thickness 3.3 - 4.5 nm
Stability
1) CTF-HUST-S5 is stable in water and ethanol.
2) Thermal decomposition temperature is above 630°C.
Preservation
1) Keep in dry and cool condition.
2) Activate by heating in vacuum at room temperature for 3 hours before use.
Other Features
Fluorescence: Yes
Applications
1) Efficient photocatalytic hydrogen evolution from seawater.
2) Potential application in visible light-driven photocatalysis.
Characterizations
XRD
NA
SEM
NA
BET
NA
FTIR
NA
References
1) Guo, Liping; Wang, Xuepeng; Zhan, Zhen; Zhao, Yueli; Chen, Linjiang; Liu, Tao; Tan, Bien; Jin, Shangbin; Chem. Mater. 2021, 33, 1994−2003, DOI: 10.1021/acs.chemmater.0c03716, Crystallization of Covalent Triazine Frameworks via a Heterogeneous Nucleation Approach for Efficient Photocatalytic Applications
1,4-Benzenedicarboximidamide, hydrochloride (1:2), polymer with thieno[3,2-b]thiophene-2,5-dicarboxaldehyde
1,4-Benzenedicarboximidamide, hydrochloride (1:2), polymer with thieno[3,2-b]thiophene-2,5-dicarboxaldehyde

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