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Novel stilbene-triazine symmetrical optical brighteners: synthesis and applications.

Journal of fluorescence

Saeed A, Shabir G, Batool I.
PMID: 24859631
J Fluoresc. 2014 Jul;24(4):1119-27. doi: 10.1007/s10895-014-1392-1. Epub 2014 May 25.

A series of new high light fastness, hot pressing fastness optical brighteners was efficiently synthesized by a three-step approach involving the successive replacement of the three chloro groups of 2,4,6-trichloro-1,3,5-triazine under different conditions of temperature and pH. Thus, 2,4,6-trichloro-1,3,5-triazine...

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Saeed A, Shabir G, Batool I. Novel stilbene-triazine symmetrical optical brighteners: synthesis and applications. J Fluoresc. 2014;24(4):1119-27doi: 10.1007/s10895-014-1392-1.
Saeed, A., Shabir, G., & Batool, I. (2014). Novel stilbene-triazine symmetrical optical brighteners: synthesis and applications. Journal of fluorescence, 24(4), 1119-27. https://doi.org/10.1007/s10895-014-1392-1
Saeed, Aamer, et al. "Novel stilbene-triazine symmetrical optical brighteners: synthesis and applications." Journal of fluorescence vol. 24,4 (2014): 1119-27. doi: https://doi.org/10.1007/s10895-014-1392-1
Saeed A, Shabir G, Batool I. Novel stilbene-triazine symmetrical optical brighteners: synthesis and applications. J Fluoresc. 2014 Jul;24(4):1119-27. doi: 10.1007/s10895-014-1392-1. Epub 2014 May 25. PMID: 24859631.
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Multichromic Bis-Axially Extended Perylene Chromophore with Schiff Bases: Synthesis, Characterization and Electrochemical Studies.

Journal of fluorescence

Shabir G, Saeed A, Arshad M, Zahid M.
PMID: 27672080
J Fluoresc. 2016 Nov;26(6):2247-2255. doi: 10.1007/s10895-016-1920-2. Epub 2016 Sep 27.

In the present paper a novel way of symmetric conjugation extension along molecular axes of perylene dianhydride chromophore has been devised to achieve lengthy delocalized electronic species exhibiting red shifted absorption and emission of UV-Visible radiations. During synthetic pathway...

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Shabir G, Saeed A, Arshad M, et al. Multichromic Bis-Axially Extended Perylene Chromophore with Schiff Bases: Synthesis, Characterization and Electrochemical Studies. J Fluoresc. 2016;26(6):2247-2255doi: 10.1007/s10895-016-1920-2.
Shabir, G., Saeed, A., Arshad, M., & Zahid, M. (2016). Multichromic Bis-Axially Extended Perylene Chromophore with Schiff Bases: Synthesis, Characterization and Electrochemical Studies. Journal of fluorescence, 26(6), 2247-2255. https://doi.org/10.1007/s10895-016-1920-2
Shabir, Ghulam, et al. "Multichromic Bis-Axially Extended Perylene Chromophore with Schiff Bases: Synthesis, Characterization and Electrochemical Studies." Journal of fluorescence vol. 26,6 (2016): 2247-2255. doi: https://doi.org/10.1007/s10895-016-1920-2
Shabir G, Saeed A, Arshad M, Zahid M. Multichromic Bis-Axially Extended Perylene Chromophore with Schiff Bases: Synthesis, Characterization and Electrochemical Studies. J Fluoresc. 2016 Nov;26(6):2247-2255. doi: 10.1007/s10895-016-1920-2. Epub 2016 Sep 27. PMID: 27672080.
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Metal Complexation Properties of Schiff Bases Containing 1,3,5-Triazine Derived from 2-Hydroxy-1-Naphthaldehyde in Solution. A Simple Spectrofluorimetric Method to Determine Mercury (II).

Journal of fluorescence

Ocak M, Ak T, Aktaş A, Özbek N, Çağılcı OC, Gümrükçüoğlu A, Kantekin H, Ocak Ü, Alp H.
PMID: 27633371
J Fluoresc. 2017 Jan;27(1):59-68. doi: 10.1007/s10895-016-1934-9. Epub 2016 Sep 16.

Four new Schiff base ligands carrying naphthalene groups were prepared from the reaction of 2,4-diamino-6-methyl-1,3,5-triazine and 2,4-diamino-6-undecyl-1,3,5-triazine with 2-hydroxy-1-naphthaldehyde. The influence of a series of metal ions including Cu

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Ocak M, Ak T, Aktaş A, et al. Metal Complexation Properties of Schiff Bases Containing 1,3,5-Triazine Derived from 2-Hydroxy-1-Naphthaldehyde in Solution. A Simple Spectrofluorimetric Method to Determine Mercury (II). J Fluoresc. 2016;27(1):59-68doi: 10.1007/s10895-016-1934-9.
Ocak, M., Ak, T., Aktaş, A., Özbek, N., Çağılcı, O. C., Gümrükçüoğlu, A., Kantekin, H., Ocak, �. �., & Alp, H. (2017). Metal Complexation Properties of Schiff Bases Containing 1,3,5-Triazine Derived from 2-Hydroxy-1-Naphthaldehyde in Solution. A Simple Spectrofluorimetric Method to Determine Mercury (II). Journal of fluorescence, 27(1), 59-68. https://doi.org/10.1007/s10895-016-1934-9
Ocak, Miraç, et al. "Metal Complexation Properties of Schiff Bases Containing 1,3,5-Triazine Derived from 2-Hydroxy-1-Naphthaldehyde in Solution. A Simple Spectrofluorimetric Method to Determine Mercury (II)." Journal of fluorescence vol. 27,1 (2017): 59-68. doi: https://doi.org/10.1007/s10895-016-1934-9
Ocak M, Ak T, Aktaş A, Özbek N, Çağılcı OC, Gümrükçüoğlu A, Kantekin H, Ocak Ü, Alp H. Metal Complexation Properties of Schiff Bases Containing 1,3,5-Triazine Derived from 2-Hydroxy-1-Naphthaldehyde in Solution. A Simple Spectrofluorimetric Method to Determine Mercury (II). J Fluoresc. 2017 Jan;27(1):59-68. doi: 10.1007/s10895-016-1934-9. Epub 2016 Sep 16. PMID: 27633371.
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Improved luminescence intensity and stability of thermal annealed ZnO incorporated Alq3 composite films.

Journal of fluorescence

Cuba M, Muralidharan G.
PMID: 26399539
J Fluoresc. 2015 Nov;25(6):1629-35. doi: 10.1007/s10895-015-1649-3. Epub 2015 Sep 23.

The 30 wt% of ZnO (weight percentage of ZnO has been optimised) incorporated tris- (8-hydroxyquinoline)aluminum (Alq3) has been synthesised and coated on to glass substrates using dip coating method. The structural and optical properties of the Alq3/ZnO composite film...

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Cuba M, Muralidharan G. Improved luminescence intensity and stability of thermal annealed ZnO incorporated Alq3 composite films. J Fluoresc. 2015;25(6):1629-35doi: 10.1007/s10895-015-1649-3.
Cuba, M., & Muralidharan, G. (2015). Improved luminescence intensity and stability of thermal annealed ZnO incorporated Alq3 composite films. Journal of fluorescence, 25(6), 1629-35. https://doi.org/10.1007/s10895-015-1649-3
Cuba, M, and Muralidharan, G. "Improved luminescence intensity and stability of thermal annealed ZnO incorporated Alq3 composite films." Journal of fluorescence vol. 25,6 (2015): 1629-35. doi: https://doi.org/10.1007/s10895-015-1649-3
Cuba M, Muralidharan G. Improved luminescence intensity and stability of thermal annealed ZnO incorporated Alq3 composite films. J Fluoresc. 2015 Nov;25(6):1629-35. doi: 10.1007/s10895-015-1649-3. Epub 2015 Sep 23. PMID: 26399539.
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Fluorescence Turn off Sensor for Brilliant Blue FCF- an Approach Based on Inner Filter Effect.

Journal of fluorescence

Sivasankaran U, Cyriac ST, Menon S, Kumar KG.
PMID: 27639570
J Fluoresc. 2017 Jan;27(1):69-77. doi: 10.1007/s10895-016-1935-8. Epub 2016 Sep 18.

A nanosensor with fluorometric readout based on L-cysteine capped cadmium sulphide quantum dots for discriminative detection and determination of Brilliant blue FCF (BB) (in 0.5 M Tris buffer solution of pH 9.5) over other synthetic food colourants is developed....

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Sivasankaran U, Cyriac ST, Menon S, et al. Fluorescence Turn off Sensor for Brilliant Blue FCF- an Approach Based on Inner Filter Effect. J Fluoresc. 2016;27(1):69-77doi: 10.1007/s10895-016-1935-8.
Sivasankaran, U., Cyriac, S. T., Menon, S., & Kumar, K. G. (2017). Fluorescence Turn off Sensor for Brilliant Blue FCF- an Approach Based on Inner Filter Effect. Journal of fluorescence, 27(1), 69-77. https://doi.org/10.1007/s10895-016-1935-8
Sivasankaran, Unni, et al. "Fluorescence Turn off Sensor for Brilliant Blue FCF- an Approach Based on Inner Filter Effect." Journal of fluorescence vol. 27,1 (2017): 69-77. doi: https://doi.org/10.1007/s10895-016-1935-8
Sivasankaran U, Cyriac ST, Menon S, Kumar KG. Fluorescence Turn off Sensor for Brilliant Blue FCF- an Approach Based on Inner Filter Effect. J Fluoresc. 2017 Jan;27(1):69-77. doi: 10.1007/s10895-016-1935-8. Epub 2016 Sep 18. PMID: 27639570.
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Fluorescent Polyamide-Based Rhodamine Hydrazide Moieties with Oxethyl as Spacer for Detection of Cr(3+), Fe(3+), and Hg(2+) Ions in Water.

Journal of fluorescence

Geng TM, Wang X, Jiang H, Song W, Ni RF, Chen J, Wang Y.
PMID: 26979056
J Fluoresc. 2016 May;26(3):977-85. doi: 10.1007/s10895-016-1785-4. Epub 2016 Mar 15.

An acrylic monomer bearing xanthene group, N-oxethyl acrylate-N'-rhodamine B hydrazide (ARBHE) was synthesized from N-hydroxyl ethyl-N'-rhodamine hydrazide (RBHE) and acryloyl chloride (Ac) in the presence of triethylamine in dry dichloromethane (CH2Cl2) at room temperature. The synthesized ARBHE was identified...

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Geng TM, Wang X, Jiang H, et al. Fluorescent Polyamide-Based Rhodamine Hydrazide Moieties with Oxethyl as Spacer for Detection of Cr(3+), Fe(3+), and Hg(2+) Ions in Water. J Fluoresc. 2016;26(3):977-85doi: 10.1007/s10895-016-1785-4.
Geng, T. M., Wang, X., Jiang, H., Song, W., Ni, R. F., Chen, J., & Wang, Y. (2016). Fluorescent Polyamide-Based Rhodamine Hydrazide Moieties with Oxethyl as Spacer for Detection of Cr(3+), Fe(3+), and Hg(2+) Ions in Water. Journal of fluorescence, 26(3), 977-85. https://doi.org/10.1007/s10895-016-1785-4
Geng, Tong-Mou, et al. "Fluorescent Polyamide-Based Rhodamine Hydrazide Moieties with Oxethyl as Spacer for Detection of Cr(3+), Fe(3+), and Hg(2+) Ions in Water." Journal of fluorescence vol. 26,3 (2016): 977-85. doi: https://doi.org/10.1007/s10895-016-1785-4
Geng TM, Wang X, Jiang H, Song W, Ni RF, Chen J, Wang Y. Fluorescent Polyamide-Based Rhodamine Hydrazide Moieties with Oxethyl as Spacer for Detection of Cr(3+), Fe(3+), and Hg(2+) Ions in Water. J Fluoresc. 2016 May;26(3):977-85. doi: 10.1007/s10895-016-1785-4. Epub 2016 Mar 15. PMID: 26979056.
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Influence of Shell Formation on Morphological Structure, Optical and Emission Intensity on Aqueous Dispersible NaYF4:Ce/Tb Nanoparticles.

Journal of fluorescence

Ansari AA, Parchur AK, Kumar B, Rai SB.
PMID: 27207570
J Fluoresc. 2016 Jul;26(4):1151-9. doi: 10.1007/s10895-016-1824-1. Epub 2016 May 20.

A highly water-dispersible NaYF4:Ce/Tb (core), NaYF4:Ce/Tb@NaYF4(core/shell) and NaYF4:Ce/Tb@NaYF4@SiO2 (core/shell/SiO2) nanoparticles (NPs) were synthesized via a general synthesis approach. The growth of an inert NaYF4 and silica shell (~14 nm) around the core-NPs resulted in an increase of the average...

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Ansari AA, Parchur AK, Kumar B, et al. Influence of Shell Formation on Morphological Structure, Optical and Emission Intensity on Aqueous Dispersible NaYF4:Ce/Tb Nanoparticles. J Fluoresc. 2016;26(4):1151-9doi: 10.1007/s10895-016-1824-1.
Ansari, A. A., Parchur, A. K., Kumar, B., & Rai, S. B. (2016). Influence of Shell Formation on Morphological Structure, Optical and Emission Intensity on Aqueous Dispersible NaYF4:Ce/Tb Nanoparticles. Journal of fluorescence, 26(4), 1151-9. https://doi.org/10.1007/s10895-016-1824-1
Ansari, Anees A, et al. "Influence of Shell Formation on Morphological Structure, Optical and Emission Intensity on Aqueous Dispersible NaYF4:Ce/Tb Nanoparticles." Journal of fluorescence vol. 26,4 (2016): 1151-9. doi: https://doi.org/10.1007/s10895-016-1824-1
Ansari AA, Parchur AK, Kumar B, Rai SB. Influence of Shell Formation on Morphological Structure, Optical and Emission Intensity on Aqueous Dispersible NaYF4:Ce/Tb Nanoparticles. J Fluoresc. 2016 Jul;26(4):1151-9. doi: 10.1007/s10895-016-1824-1. Epub 2016 May 20. PMID: 27207570.
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Study on Synthesis and Fluorescence of Novel Benzofused Phenazine π-Conjugated Skeleton with Coumarin and Isophoron Cores.

Journal of fluorescence

Choudhary AS, Patil SR, Sekar N.
PMID: 26139529
J Fluoresc. 2015 Jul;25(4):1095-102. doi: 10.1007/s10895-015-1597-y. Epub 2015 Jul 03.

The novel benzofused phenazine π-conjugated skeleton with a coumarin and isophoron core was synthesized, characterized, and condensed with suitably substituted active methylene compounds by classical Knoevenagel condensation reaction to obtain novel mono-styryl dyes 6a-6d. These novel styryl dyes have...

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Choudhary AS, Patil SR, Sekar N. Study on Synthesis and Fluorescence of Novel Benzofused Phenazine π-Conjugated Skeleton with Coumarin and Isophoron Cores. J Fluoresc. 2015;25(4):1095-102doi: 10.1007/s10895-015-1597-y.
Choudhary, A. S., Patil, S. R., & Sekar, N. (2015). Study on Synthesis and Fluorescence of Novel Benzofused Phenazine π-Conjugated Skeleton with Coumarin and Isophoron Cores. Journal of fluorescence, 25(4), 1095-102. https://doi.org/10.1007/s10895-015-1597-y
Choudhary, Amol S, et al. "Study on Synthesis and Fluorescence of Novel Benzofused Phenazine π-Conjugated Skeleton with Coumarin and Isophoron Cores." Journal of fluorescence vol. 25,4 (2015): 1095-102. doi: https://doi.org/10.1007/s10895-015-1597-y
Choudhary AS, Patil SR, Sekar N. Study on Synthesis and Fluorescence of Novel Benzofused Phenazine π-Conjugated Skeleton with Coumarin and Isophoron Cores. J Fluoresc. 2015 Jul;25(4):1095-102. doi: 10.1007/s10895-015-1597-y. Epub 2015 Jul 03. PMID: 26139529.
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Fluorescence and Textural Characterization of Ortho-Amine Tetraphenylporphyrin Covalently Bonded to Organo-Modified Silica Xerogels.

Journal of fluorescence

García-Sánchez MA, Serratos IN, Sosa R, Rojas-González F, Tello-Solís SR, Tapia-Esquivel T, González-García F, Esparza-Schulz JM, Huerta-Figueroa DE.
PMID: 27324951
J Fluoresc. 2016 Sep;26(5):1601-16. doi: 10.1007/s10895-016-1846-8. Epub 2016 Jun 20.

Most of the studies performed with porphyrins involve these species functionalized with peripheral substituents lying on the same macrocyclic molecular plane. The main objective of this work deals with the successful preservation and optimization of the fluorescence of a...

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García-Sánchez MA, Serratos IN, Sosa R, et al. Fluorescence and Textural Characterization of Ortho-Amine Tetraphenylporphyrin Covalently Bonded to Organo-Modified Silica Xerogels. J Fluoresc. 2016;26(5):1601-16doi: 10.1007/s10895-016-1846-8.
García-Sánchez, M. A., Serratos, I. N., Sosa, R., Rojas-González, F., Tello-Solís, S. R., Tapia-Esquivel, T., González-García, F., Esparza-Schulz, J. M., & Huerta-Figueroa, D. E. (2016). Fluorescence and Textural Characterization of Ortho-Amine Tetraphenylporphyrin Covalently Bonded to Organo-Modified Silica Xerogels. Journal of fluorescence, 26(5), 1601-16. https://doi.org/10.1007/s10895-016-1846-8
García-Sánchez, M A, et al. "Fluorescence and Textural Characterization of Ortho-Amine Tetraphenylporphyrin Covalently Bonded to Organo-Modified Silica Xerogels." Journal of fluorescence vol. 26,5 (2016): 1601-16. doi: https://doi.org/10.1007/s10895-016-1846-8
García-Sánchez MA, Serratos IN, Sosa R, Rojas-González F, Tello-Solís SR, Tapia-Esquivel T, González-García F, Esparza-Schulz JM, Huerta-Figueroa DE. Fluorescence and Textural Characterization of Ortho-Amine Tetraphenylporphyrin Covalently Bonded to Organo-Modified Silica Xerogels. J Fluoresc. 2016 Sep;26(5):1601-16. doi: 10.1007/s10895-016-1846-8. Epub 2016 Jun 20. PMID: 27324951.
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Enhance Efficiency of Solar Cell Using Luminescence PbS Quantum Dots Concentrators.

Journal of fluorescence

Reda SM.
PMID: 25740343
J Fluoresc. 2015 May;25(3):631-9. doi: 10.1007/s10895-015-1546-9. Epub 2015 Mar 05.

Thin film and sheet PbS quantum dots (QDs) concentrators were synthesized by sol-gel method using three different PbS concentrations (0.14, 0.2, and 0.4 mol%). The structure and morphology of the prepared PbS QDs were characterized by X-ray diffraction (XRD),...

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Reda SM. Enhance Efficiency of Solar Cell Using Luminescence PbS Quantum Dots Concentrators. J Fluoresc. 2015;25(3):631-9doi: 10.1007/s10895-015-1546-9.
Reda, S. M. (2015). Enhance Efficiency of Solar Cell Using Luminescence PbS Quantum Dots Concentrators. Journal of fluorescence, 25(3), 631-9. https://doi.org/10.1007/s10895-015-1546-9
Reda, S M. "Enhance Efficiency of Solar Cell Using Luminescence PbS Quantum Dots Concentrators." Journal of fluorescence vol. 25,3 (2015): 631-9. doi: https://doi.org/10.1007/s10895-015-1546-9
Reda SM. Enhance Efficiency of Solar Cell Using Luminescence PbS Quantum Dots Concentrators. J Fluoresc. 2015 May;25(3):631-9. doi: 10.1007/s10895-015-1546-9. Epub 2015 Mar 05. PMID: 25740343.
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A Facile Method for the Synthesis Fluorescent Zinc Chalcogenide (ZnO, ZnS and ZnSe) Nanoparticles in PS and PMMA Polymer Matrix.

Journal of fluorescence

Hariharan PS, Subhashini N, Vasanthalakshmi J, Anthony SP.
PMID: 26753757
J Fluoresc. 2016 Mar;26(2):703-7. doi: 10.1007/s10895-015-1757-0. Epub 2016 Jan 11.

A simple method for the synthesis of fluorescent zinc chalcogenide (ZnO, ZnS and ZnSe) nanoparticles directly in the transparent PMMA and PS polymer matrices were reported. Highly dispersed small spherical ZnO nanoparticles (3-5 nm) was obtained by hydrothermal reaction...

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Hariharan PS, Subhashini N, Vasanthalakshmi J, et al. A Facile Method for the Synthesis Fluorescent Zinc Chalcogenide (ZnO, ZnS and ZnSe) Nanoparticles in PS and PMMA Polymer Matrix. J Fluoresc. 2016;26(2):703-7doi: 10.1007/s10895-015-1757-0.
Hariharan, P. S., Subhashini, N., Vasanthalakshmi, J., & Anthony, S. P. (2016). A Facile Method for the Synthesis Fluorescent Zinc Chalcogenide (ZnO, ZnS and ZnSe) Nanoparticles in PS and PMMA Polymer Matrix. Journal of fluorescence, 26(2), 703-7. https://doi.org/10.1007/s10895-015-1757-0
Hariharan, P S, et al. "A Facile Method for the Synthesis Fluorescent Zinc Chalcogenide (ZnO, ZnS and ZnSe) Nanoparticles in PS and PMMA Polymer Matrix." Journal of fluorescence vol. 26,2 (2016): 703-7. doi: https://doi.org/10.1007/s10895-015-1757-0
Hariharan PS, Subhashini N, Vasanthalakshmi J, Anthony SP. A Facile Method for the Synthesis Fluorescent Zinc Chalcogenide (ZnO, ZnS and ZnSe) Nanoparticles in PS and PMMA Polymer Matrix. J Fluoresc. 2016 Mar;26(2):703-7. doi: 10.1007/s10895-015-1757-0. Epub 2016 Jan 11. PMID: 26753757.
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Fluorescence Titrations of Bio-relevant Complexes with DNA: Synthesis, Structural Investigation, DNA Binding/Cleavage, Antimicrobial and Molecular Docking Studies.

Journal of fluorescence

Arun TR, Subramanian R, Packianathan S, Raman N.
PMID: 26149500
J Fluoresc. 2015 Jul;25(4):1127-40. doi: 10.1007/s10895-015-1603-4. Epub 2015 Jul 07.

In the present work, we attempted to develop new metal complexes (Cu(II), Co(II), Ni(II) and Zn(II)) of the imine ligand which was synthesized from 9,10-phenanthrenequinone and para-anisidine. With an intention to make the complexes most stable, very special chelating...

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Arun TR, Subramanian R, Packianathan S, et al. Fluorescence Titrations of Bio-relevant Complexes with DNA: Synthesis, Structural Investigation, DNA Binding/Cleavage, Antimicrobial and Molecular Docking Studies. J Fluoresc. 2015;25(4):1127-40doi: 10.1007/s10895-015-1603-4.
Arun, T. R., Subramanian, R., Packianathan, S., & Raman, N. (2015). Fluorescence Titrations of Bio-relevant Complexes with DNA: Synthesis, Structural Investigation, DNA Binding/Cleavage, Antimicrobial and Molecular Docking Studies. Journal of fluorescence, 25(4), 1127-40. https://doi.org/10.1007/s10895-015-1603-4
Arun, Thesingu Rajan, et al. "Fluorescence Titrations of Bio-relevant Complexes with DNA: Synthesis, Structural Investigation, DNA Binding/Cleavage, Antimicrobial and Molecular Docking Studies." Journal of fluorescence vol. 25,4 (2015): 1127-40. doi: https://doi.org/10.1007/s10895-015-1603-4
Arun TR, Subramanian R, Packianathan S, Raman N. Fluorescence Titrations of Bio-relevant Complexes with DNA: Synthesis, Structural Investigation, DNA Binding/Cleavage, Antimicrobial and Molecular Docking Studies. J Fluoresc. 2015 Jul;25(4):1127-40. doi: 10.1007/s10895-015-1603-4. Epub 2015 Jul 07. PMID: 26149500.
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