2007
DOI: 10.1016/j.optmat.2007.01.014
|View full text |Cite
|
Sign up to set email alerts
|

Studies on the growth, optical, thermal and dielectric aspects of a proton transfer complex – Dimethyl amino pyridinium 4-nitrophenolate 4-nitrophenol (DMAPNP) crystals for non-linear optical applications

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
17
0

Year Published

2010
2010
2019
2019

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 65 publications
(17 citation statements)
references
References 34 publications
0
17
0
Order By: Relevance
“…Crystals were grown by slow evaporation technique at a fixed temperature. This technique is widely used by several groups of scientists [8][9][10][11][12][17][18][19]. We followed the synthetic procedure of co-crystals production with 4-nitrophenol that was published by Prakash et al [8].…”
Section: Synthesis and Crystal Growthmentioning
confidence: 99%
“…Crystals were grown by slow evaporation technique at a fixed temperature. This technique is widely used by several groups of scientists [8][9][10][11][12][17][18][19]. We followed the synthetic procedure of co-crystals production with 4-nitrophenol that was published by Prakash et al [8].…”
Section: Synthesis and Crystal Growthmentioning
confidence: 99%
“…IR spectral data for pure 2-, 3-, and 4-nitrophenol and 2-, 3-, and 4-nitrophenol adsorbed ammonium Y zeolite are listed in Table 2. We refer to works [15][16][17][18][19][20][21][22][23][24][25][26] for vibrational assignments of 2-nitrophenol, [15][16][17][18][19][20][21]24,27] for vibrational assignments of 3-nitrophenol, [15][16][17][18][19][20][21][22][23][24][25][26]28] for vibrational assignments of 4-nitrophenol. Table 2 lists the wavenumbers of the observed bands as well as their assignment based on the PED calculations, where the contributions are organized according to the main molecular groups of 2-, 3-, and 4-nitrophenol neglecting group contributions lower than 10%.…”
Section: Fourier Transform Infrared Spectroscopic Resultsmentioning
confidence: 99%
“…The protonation and the consequential positive charge on the ring nitrogen of this pyridine derivative construct the heteroatom as a strong electron acceptor, and it is habitually used which evade to utilize of non-linear optics chromophores in uncontaminated enantiomeric form through donor-acceptor cocrystalization [9][10][11][12][13]. This base can be introduced into multicomponent crystals to tune the luminescent properties of an organic fluorescent dye through rational control of the interaction and arrangement of chromophores within the crystal [14].…”
Section: Commentmentioning
confidence: 99%