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Synthesis, solvatochromism and crystal structure of 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H -1,2,4-triazine-3-thione.

Rezaei B, Fazlollahi M - Chem Cent J (2013)

Bottom Line: It was found that the monomer of the ligand 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione, further extends into 3D networks via hydrogen bonding and pi-pi stacking interactions.While progressing from the non-polar solvent to the polar one, the main intense band at 310 nm, which is due to the π-π* transition, was red shifted by 13 nm.Thus, the title compound showed positive solvatochromic behavior.

View Article: PubMed Central - HTML - PubMed

Affiliation: Department of Chemistry, Lorestan University, Khorramabad, Iran.

ABSTRACT

Background: For the development of properties in molecular crystals, such as electrical conductivities, magnetic properties, or non-linear optical properties, not only the electronic properties of molecules themselves matter, but also the molecular arrangements in the crystals are very important. Therefore, the design of the crystal structures and the control of molecular arrangements have attracted much attention in recent years. Among various ligands, triazine moieties have been especially interesting because of their biological, pharmacological and medicinal properties.

Results: Crystal structure of 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione is Monoclinic, which consists of space group P21/c with a = 9.699(1), b = 8.500(1), c = 18.044(2) Å, β = 101.290(7)° and Z = 4, R1 = 0.0371 and wR2 = 0.1008 with 2456 reflections (I > 2σ(I)). Intermolecular H bonds between NH groups are acting as donors and S atoms as acceptors. There are also shorted face-to-face as well as edge to face π-π stacking interactions between the parallel aromatic rings. The behavior of solvatochromic of the mentioned compound that involved interhydrogen bonding was investigated by studying its electronic absorption spectra in pure organic solvents of different characters.

Conclusions: The crystal structure of C16H15N3OS, shows the expected face-to-face π-π stacking interactions between aromatic rings of the neighbor chains in this compound. The centroid-centroid distance between the aromatic rings is 3.325 Å. It was found that the monomer of the ligand 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione, further extends into 3D networks via hydrogen bonding and pi-pi stacking interactions. The solvatochromic behavior of the title compound was also investigated by studying its spectra in a selection of different organic solvents. While progressing from the non-polar solvent to the polar one, the main intense band at 310 nm, which is due to the π-π* transition, was red shifted by 13 nm. Thus, the title compound showed positive solvatochromic behavior.

No MeSH data available.


Related in: MedlinePlus

The electronic absorption spectra of a 3.8 × 10-5 mol liter-1 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione in organic solvents:(1)C6H12 (2)CCl4 (3)CHCl3 (4)EtOH (5)MeOH (6)DMF (7)CH3CN (8)DMSO.
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Figure 4: The electronic absorption spectra of a 3.8 × 10-5 mol liter-1 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione in organic solvents:(1)C6H12 (2)CCl4 (3)CHCl3 (4)EtOH (5)MeOH (6)DMF (7)CH3CN (8)DMSO.

Mentions: The electronic absorption spectra of 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione was studied in organic solvents of different polarities, viz. Hexane, CCl4, CHCl3, C2H5OH, CH3OH, DMF, CH3CN, DMSO (Figure 4). This was done with the intention to investigate the solvatochromic behavior of this compound. While moving from the non-polar solvent to the polar one, the main intense band at 310 nm, which is due to the (π–π*) transition, is red shifted by 13 nm. Therefore, the absorption band of the title compound corresponding to the π–π* transition, shifts to longer wavelengths with an increase of dielectric constant of the solvents. This suggests stabilization of the electronic excited state relative to the ground state. Thus, the title compound showed positive solvatochromic behavior [9,10].


Synthesis, solvatochromism and crystal structure of 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H -1,2,4-triazine-3-thione.

Rezaei B, Fazlollahi M - Chem Cent J (2013)

The electronic absorption spectra of a 3.8 × 10-5 mol liter-1 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione in organic solvents:(1)C6H12 (2)CCl4 (3)CHCl3 (4)EtOH (5)MeOH (6)DMF (7)CH3CN (8)DMSO.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC3750551&req=5

Figure 4: The electronic absorption spectra of a 3.8 × 10-5 mol liter-1 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione in organic solvents:(1)C6H12 (2)CCl4 (3)CHCl3 (4)EtOH (5)MeOH (6)DMF (7)CH3CN (8)DMSO.
Mentions: The electronic absorption spectra of 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione was studied in organic solvents of different polarities, viz. Hexane, CCl4, CHCl3, C2H5OH, CH3OH, DMF, CH3CN, DMSO (Figure 4). This was done with the intention to investigate the solvatochromic behavior of this compound. While moving from the non-polar solvent to the polar one, the main intense band at 310 nm, which is due to the (π–π*) transition, is red shifted by 13 nm. Therefore, the absorption band of the title compound corresponding to the π–π* transition, shifts to longer wavelengths with an increase of dielectric constant of the solvents. This suggests stabilization of the electronic excited state relative to the ground state. Thus, the title compound showed positive solvatochromic behavior [9,10].

Bottom Line: It was found that the monomer of the ligand 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione, further extends into 3D networks via hydrogen bonding and pi-pi stacking interactions.While progressing from the non-polar solvent to the polar one, the main intense band at 310 nm, which is due to the π-π* transition, was red shifted by 13 nm.Thus, the title compound showed positive solvatochromic behavior.

View Article: PubMed Central - HTML - PubMed

Affiliation: Department of Chemistry, Lorestan University, Khorramabad, Iran.

ABSTRACT

Background: For the development of properties in molecular crystals, such as electrical conductivities, magnetic properties, or non-linear optical properties, not only the electronic properties of molecules themselves matter, but also the molecular arrangements in the crystals are very important. Therefore, the design of the crystal structures and the control of molecular arrangements have attracted much attention in recent years. Among various ligands, triazine moieties have been especially interesting because of their biological, pharmacological and medicinal properties.

Results: Crystal structure of 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione is Monoclinic, which consists of space group P21/c with a = 9.699(1), b = 8.500(1), c = 18.044(2) Å, β = 101.290(7)° and Z = 4, R1 = 0.0371 and wR2 = 0.1008 with 2456 reflections (I > 2σ(I)). Intermolecular H bonds between NH groups are acting as donors and S atoms as acceptors. There are also shorted face-to-face as well as edge to face π-π stacking interactions between the parallel aromatic rings. The behavior of solvatochromic of the mentioned compound that involved interhydrogen bonding was investigated by studying its electronic absorption spectra in pure organic solvents of different characters.

Conclusions: The crystal structure of C16H15N3OS, shows the expected face-to-face π-π stacking interactions between aromatic rings of the neighbor chains in this compound. The centroid-centroid distance between the aromatic rings is 3.325 Å. It was found that the monomer of the ligand 5-Methoxy-5,6-diphenyl-4,5-dihydro-2H-1,2,4-triazine-3-thione, further extends into 3D networks via hydrogen bonding and pi-pi stacking interactions. The solvatochromic behavior of the title compound was also investigated by studying its spectra in a selection of different organic solvents. While progressing from the non-polar solvent to the polar one, the main intense band at 310 nm, which is due to the π-π* transition, was red shifted by 13 nm. Thus, the title compound showed positive solvatochromic behavior.

No MeSH data available.


Related in: MedlinePlus