Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 79 entries
Sorted by: Best Match Show Resources per page
Going beyond red with a tri- and tetracoordinate boron conjugate: intriguing near-IR optical properties and applications in anion sensing.

Inorganic chemistry

Sarkar SK, Mukherjee S, Thilagar P.
PMID: 24520954
Inorg Chem. 2014 Mar 03;53(5):2343-5. doi: 10.1021/ic402441w. Epub 2014 Feb 13.

The design and synthesis of a new tri- and tetracoordinate boron conjugate is reported. The conjugate shows broad near-IR emission (∼625-850 nm) and is found to be a selective colorimetric and ratiometric sensor for fluoride ions.

Cite
Sarkar SK, Mukherjee S, Thilagar P. Going beyond red with a tri- and tetracoordinate boron conjugate: intriguing near-IR optical properties and applications in anion sensing. Inorg Chem. 2014;53(5):2343-5doi: 10.1021/ic402441w.
Sarkar, S. K., Mukherjee, S., & Thilagar, P. (2014). Going beyond red with a tri- and tetracoordinate boron conjugate: intriguing near-IR optical properties and applications in anion sensing. Inorganic chemistry, 53(5), 2343-5. https://doi.org/10.1021/ic402441w
Sarkar, Samir Kumar, et al. "Going beyond red with a tri- and tetracoordinate boron conjugate: intriguing near-IR optical properties and applications in anion sensing." Inorganic chemistry vol. 53,5 (2014): 2343-5. doi: https://doi.org/10.1021/ic402441w
Sarkar SK, Mukherjee S, Thilagar P. Going beyond red with a tri- and tetracoordinate boron conjugate: intriguing near-IR optical properties and applications in anion sensing. Inorg Chem. 2014 Mar 03;53(5):2343-5. doi: 10.1021/ic402441w. Epub 2014 Feb 13. PMID: 24520954.
Copy Download .nbib Format: NLM
Triarylborane conjugated dicyanovinyl chromophores: intriguing optical properties and colorimetric anion discrimination.

Physical chemistry chemical physics : PCCP

Kumar GR, Sarkar SK, Thilagar P.
PMID: 26509424
Phys Chem Chem Phys. 2015 Nov 11;17(45):30424-32. doi: 10.1039/c5cp05378a.

Three new triarylborane conjugated dicyanovinyl chromophores (Mes2B-π-donor-DCV); donor: N-methyldiphenylamine () and triphenylamine ( and [with two BMes2 substitutions]) of type A-D-A (acceptor-donor-acceptor) are reported. Compounds exhibit intense charge transfer (CT) absorption bands in the visible region. These absorption peaks...

Cite
Kumar GR, Sarkar SK, Thilagar P. Triarylborane conjugated dicyanovinyl chromophores: intriguing optical properties and colorimetric anion discrimination. Phys Chem Chem Phys. 2015;17(45):30424-32doi: 10.1039/c5cp05378a.
Kumar, G. R., Sarkar, S. K., & Thilagar, P. (2015). Triarylborane conjugated dicyanovinyl chromophores: intriguing optical properties and colorimetric anion discrimination. Physical chemistry chemical physics : PCCP, 17(45), 30424-32. https://doi.org/10.1039/c5cp05378a
Kumar, George Rajendra, et al. "Triarylborane conjugated dicyanovinyl chromophores: intriguing optical properties and colorimetric anion discrimination." Physical chemistry chemical physics : PCCP vol. 17,45 (2015): 30424-32. doi: https://doi.org/10.1039/c5cp05378a
Kumar GR, Sarkar SK, Thilagar P. Triarylborane conjugated dicyanovinyl chromophores: intriguing optical properties and colorimetric anion discrimination. Phys Chem Chem Phys. 2015 Nov 11;17(45):30424-32. doi: 10.1039/c5cp05378a. PMID: 26509424.
Copy Download .nbib Format: NLM
Multichannel-emissive V-shaped boryl-BODIPY dyads: synthesis, structure, and remarkably diverse response toward fluoride.

Inorganic chemistry

Swamy P CA, Mukherjee S, Thilagar P.
PMID: 24801770
Inorg Chem. 2014 May 19;53(10):4813-23. doi: 10.1021/ic402470a. Epub 2014 May 06.

Three new V-shaped boryl-BODIPY dyads (1-3) were synthesized and structurally characterized. Compounds 1-3 are structurally close molecular siblings differing only in the number of methyl substituents on the BODIPY moiety that were found to play a major role in...

Cite
Swamy P CA, Mukherjee S, Thilagar P. Multichannel-emissive V-shaped boryl-BODIPY dyads: synthesis, structure, and remarkably diverse response toward fluoride. Inorg Chem. 2014;53(10):4813-23doi: 10.1021/ic402470a.
Swamy P, C. A., Mukherjee, S., & Thilagar, P. (2014). Multichannel-emissive V-shaped boryl-BODIPY dyads: synthesis, structure, and remarkably diverse response toward fluoride. Inorganic chemistry, 53(10), 4813-23. https://doi.org/10.1021/ic402470a
Swamy P, Chinna Ayya, et al. "Multichannel-emissive V-shaped boryl-BODIPY dyads: synthesis, structure, and remarkably diverse response toward fluoride." Inorganic chemistry vol. 53,10 (2014): 4813-23. doi: https://doi.org/10.1021/ic402470a
Swamy P CA, Mukherjee S, Thilagar P. Multichannel-emissive V-shaped boryl-BODIPY dyads: synthesis, structure, and remarkably diverse response toward fluoride. Inorg Chem. 2014 May 19;53(10):4813-23. doi: 10.1021/ic402470a. Epub 2014 May 06. PMID: 24801770.
Copy Download .nbib Format: NLM
Inorganic-cored photoactive assemblies: synthesis, structure, and photochemical investigations on stannoxane-supported multifluorene compounds.

Chemistry (Weinheim an der Bergstrasse, Germany)

Chandrasekhar V, Thilagar P, Steiner A, Bickley JF.
PMID: 16952130
Chemistry. 2006 Nov 24;12(34):8847-61. doi: 10.1002/chem.200600556.

Organostannoxanes were used as inert supports for the preparation of multichromophore assemblies. The synthesis involves a single-step procedure and allows the preparation of compounds in which the number of chromophore units can be varied from one to six. Thus,...

Cite
Chandrasekhar V, Thilagar P, Steiner A, et al. Inorganic-cored photoactive assemblies: synthesis, structure, and photochemical investigations on stannoxane-supported multifluorene compounds. Chemistry. 2006;12(34):8847-61doi: 10.1002/chem.200600556.
Chandrasekhar, V., Thilagar, P., Steiner, A., & Bickley, J. F. (2006). Inorganic-cored photoactive assemblies: synthesis, structure, and photochemical investigations on stannoxane-supported multifluorene compounds. Chemistry (Weinheim an der Bergstrasse, Germany), 12(34), 8847-61. https://doi.org/10.1002/chem.200600556
Chandrasekhar, Vadapalli, et al. "Inorganic-cored photoactive assemblies: synthesis, structure, and photochemical investigations on stannoxane-supported multifluorene compounds." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 12,34 (2006): 8847-61. doi: https://doi.org/10.1002/chem.200600556
Chandrasekhar V, Thilagar P, Steiner A, Bickley JF. Inorganic-cored photoactive assemblies: synthesis, structure, and photochemical investigations on stannoxane-supported multifluorene compounds. Chemistry. 2006 Nov 24;12(34):8847-61. doi: 10.1002/chem.200600556. PMID: 16952130.
Copy Download .nbib Format: NLM
Geometrical phases of excitonic qubits in quantum dots.

Journal of physics. Condensed matter : an Institute of Physics journal

Thilagam A.
PMID: 21715810
J Phys Condens Matter. 2009 Jan 28;21(4):045504. doi: 10.1088/0953-8984/21/4/045504. Epub 2008 Dec 19.

We investigate the influence of phonon mediated interactions on the non-unitary evolution of geometrical phases in excitonic qubits formed in quantum dots entangled by pure Förster coupling. We consider decoherence to occur via acoustic phonons interacting through the deformation...

Cite
Thilagam A. Geometrical phases of excitonic qubits in quantum dots. J Phys Condens Matter. 2008;21(4):045504doi: 10.1088/0953-8984/21/4/045504.
Thilagam, A. (2009). Geometrical phases of excitonic qubits in quantum dots. Journal of physics. Condensed matter : an Institute of Physics journal, 21(4), 045504. https://doi.org/10.1088/0953-8984/21/4/045504
Thilagam, A. "Geometrical phases of excitonic qubits in quantum dots." Journal of physics. Condensed matter : an Institute of Physics journal vol. 21,4 (2009): 045504. doi: https://doi.org/10.1088/0953-8984/21/4/045504
Thilagam A. Geometrical phases of excitonic qubits in quantum dots. J Phys Condens Matter. 2009 Jan 28;21(4):045504. doi: 10.1088/0953-8984/21/4/045504. Epub 2008 Dec 19. PMID: 21715810.
Copy Download .nbib Format: NLM
Modulation and Interaction of Immune-Associated Parameters with Antioxidant in the Immunocytes of Crab Scylla paramamosain Challenged with Lipopolysaccharides.

Evidence-based complementary and alternative medicine : eCAM

Gopalakrishnan S, Chen FY, Thilagam H, Qiao K, Xu WF, Wang KJ.
PMID: 21716691
Evid Based Complement Alternat Med. 2011;2011:824962. doi: 10.1155/2011/824962. Epub 2011 Jun 05.

Invertebrates are dependent on cellular and humoral immune defences against microbial infection. Scylla paramamosain is an important commercial species, but the fundamental knowledge on its immune defense related to the antioxidant and immune-associated reactions is still lacking. The study...

Cite
Gopalakrishnan S, Chen FY, Thilagam H, et al. Modulation and Interaction of Immune-Associated Parameters with Antioxidant in the Immunocytes of Crab Scylla paramamosain Challenged with Lipopolysaccharides. Evid Based Complement Alternat Med. 2011;2011:824962doi: 10.1155/2011/824962.
Gopalakrishnan, S., Chen, F. Y., Thilagam, H., Qiao, K., Xu, W. F., & Wang, K. J. (2011). Modulation and Interaction of Immune-Associated Parameters with Antioxidant in the Immunocytes of Crab Scylla paramamosain Challenged with Lipopolysaccharides. Evidence-based complementary and alternative medicine : eCAM, 2011824962. https://doi.org/10.1155/2011/824962
Gopalakrishnan, Singaram, et al. "Modulation and Interaction of Immune-Associated Parameters with Antioxidant in the Immunocytes of Crab Scylla paramamosain Challenged with Lipopolysaccharides." Evidence-based complementary and alternative medicine : eCAM vol. 2011 (2011): 824962. doi: https://doi.org/10.1155/2011/824962
Gopalakrishnan S, Chen FY, Thilagam H, Qiao K, Xu WF, Wang KJ. Modulation and Interaction of Immune-Associated Parameters with Antioxidant in the Immunocytes of Crab Scylla paramamosain Challenged with Lipopolysaccharides. Evid Based Complement Alternat Med. 2011;2011:824962. doi: 10.1155/2011/824962. Epub 2011 Jun 05. PMID: 21716691; PMCID: PMC3118543.
Copy Download .nbib Format: NLM
Molecular flexibility tuned emission in "V" shaped naphthalimides: Hg(II) detection and aggregation-induced emission enhancement (AIEE).

Chemical communications (Cambridge, England)

Mukherjee S, Thilagar P.
PMID: 23846300
Chem Commun (Camb). 2013 Aug 25;49(66):7292-4. doi: 10.1039/c3cc43351j.

Four "V" shaped 1,8-naphthalimides (1-4) have been synthesized and their fluorescence quantum-yields correlated to their molecular flexibility. The correlation was used for detection of Hg(II) via a chemodosimetric approach. was found to be an AIE active molecule with the...

Cite
Mukherjee S, Thilagar P. Molecular flexibility tuned emission in "V" shaped naphthalimides: Hg(II) detection and aggregation-induced emission enhancement (AIEE). Chem Commun (Camb). 2013;49(66):7292-4doi: 10.1039/c3cc43351j.
Mukherjee, S., & Thilagar, P. (2013). Molecular flexibility tuned emission in "V" shaped naphthalimides: Hg(II) detection and aggregation-induced emission enhancement (AIEE). Chemical communications (Cambridge, England), 49(66), 7292-4. https://doi.org/10.1039/c3cc43351j
Mukherjee, Sanjoy, and Thilagar, Pakkirisamy. "Molecular flexibility tuned emission in "V" shaped naphthalimides: Hg(II) detection and aggregation-induced emission enhancement (AIEE)." Chemical communications (Cambridge, England) vol. 49,66 (2013): 7292-4. doi: https://doi.org/10.1039/c3cc43351j
Mukherjee S, Thilagar P. Molecular flexibility tuned emission in "V" shaped naphthalimides: Hg(II) detection and aggregation-induced emission enhancement (AIEE). Chem Commun (Camb). 2013 Aug 25;49(66):7292-4. doi: 10.1039/c3cc43351j. PMID: 23846300.
Copy Download .nbib Format: NLM
Epizootiology, pathogenesis and immunoprophylactic trends to control tropical bubaline fasciolosis: an overview.

Journal of parasitic diseases : official organ of the Indian Society for Parasitology

Sharma RL, Godara R, Thilagar MB.
PMID: 22654308
J Parasit Dis. 2011 Jun;35(1):1-9. doi: 10.1007/s12639-011-0025-8. Epub 2011 Mar 25.

On the Indian sub-continent, nearly 5,000 years ago, the domestication of the riverine buffalo-the incredible Asian dairy animal was initiated. It plays a versatile role in socio-economic upliftment of its owners from the rural agricultural communities in Asian, African,...

Cite
Sharma RL, Godara R, Thilagar MB. Epizootiology, pathogenesis and immunoprophylactic trends to control tropical bubaline fasciolosis: an overview. J Parasit Dis. 2011;35(1):1-9doi: 10.1007/s12639-011-0025-8.
Sharma, R. L., Godara, R., & Thilagar, M. B. (2011). Epizootiology, pathogenesis and immunoprophylactic trends to control tropical bubaline fasciolosis: an overview. Journal of parasitic diseases : official organ of the Indian Society for Parasitology, 35(1), 1-9. https://doi.org/10.1007/s12639-011-0025-8
Sharma, R L, et al. "Epizootiology, pathogenesis and immunoprophylactic trends to control tropical bubaline fasciolosis: an overview." Journal of parasitic diseases : official organ of the Indian Society for Parasitology vol. 35,1 (2011): 1-9. doi: https://doi.org/10.1007/s12639-011-0025-8
Sharma RL, Godara R, Thilagar MB. Epizootiology, pathogenesis and immunoprophylactic trends to control tropical bubaline fasciolosis: an overview. J Parasit Dis. 2011 Jun;35(1):1-9. doi: 10.1007/s12639-011-0025-8. Epub 2011 Mar 25. PMID: 22654308; PMCID: PMC3114980.
Copy Download .nbib Format: NLM
Polarons in quasi-two-dimensional structures.

Physical review. B, Condensed matter

Singh J, Thilagam A.
PMID: 10010295
Phys Rev B Condens Matter. 1994 May 15;49(19):13583-13588. doi: 10.1103/physrevb.49.13583.

No abstract available.

Cite
Singh J, Thilagam A. Polarons in quasi-two-dimensional structures. Phys Rev B Condens Matter. 1994;49(19):13583-13588doi: 10.1103/physrevb.49.13583.
Singh, J., & Thilagam, A. (1994). Polarons in quasi-two-dimensional structures. Physical review. B, Condensed matter, 49(19), 13583-13588. https://doi.org/10.1103/physrevb.49.13583
Singh, and Thilagam. "Polarons in quasi-two-dimensional structures." Physical review. B, Condensed matter vol. 49,19 (1994): 13583-13588. doi: https://doi.org/10.1103/physrevb.49.13583
Singh J, Thilagam A. Polarons in quasi-two-dimensional structures. Phys Rev B Condens Matter. 1994 May 15;49(19):13583-13588. doi: 10.1103/physrevb.49.13583. PMID: 10010295.
Copy Download .nbib Format: NLM
Effect of Branching on the Delayed Fluorescence and Phosphorescence of Simple Borylated Arylamines.

Inorganic chemistry

Pagidi S, Kalluvettukuzhy NK, Thilagar P.
PMID: 32040299
Inorg Chem. 2020 Mar 02;59(5):3142-3151. doi: 10.1021/acs.inorgchem.9b03446. Epub 2020 Feb 10.

A donor-π-acceptor strategy is being well exploited in several fields in view of their robust optical properties. However, the impact of branching in quadrupolar [A-(π-D)

Cite
Pagidi S, Kalluvettukuzhy NK, Thilagar P. Effect of Branching on the Delayed Fluorescence and Phosphorescence of Simple Borylated Arylamines. Inorg Chem. 2020;59(5):3142-3151doi: 10.1021/acs.inorgchem.9b03446.
Pagidi, S., Kalluvettukuzhy, N. K., & Thilagar, P. (2020). Effect of Branching on the Delayed Fluorescence and Phosphorescence of Simple Borylated Arylamines. Inorganic chemistry, 59(5), 3142-3151. https://doi.org/10.1021/acs.inorgchem.9b03446
Pagidi, Sudhakar, et al. "Effect of Branching on the Delayed Fluorescence and Phosphorescence of Simple Borylated Arylamines." Inorganic chemistry vol. 59,5 (2020): 3142-3151. doi: https://doi.org/10.1021/acs.inorgchem.9b03446
Pagidi S, Kalluvettukuzhy NK, Thilagar P. Effect of Branching on the Delayed Fluorescence and Phosphorescence of Simple Borylated Arylamines. Inorg Chem. 2020 Mar 02;59(5):3142-3151. doi: 10.1021/acs.inorgchem.9b03446. Epub 2020 Feb 10. PMID: 32040299.
Copy Download .nbib Format: NLM
Triarylborane-Appended Anils and Boranils: Solid-State Emission, Mechanofluorochromism, and Phosphorescence.

Chemistry (Weinheim an der Bergstrasse, Germany)

Nandi RP, Sudhakar P, Kalluvettukuzhy NK, Thilagar P.
PMID: 32578898
Chemistry. 2020 Dec 09;26(69):16306-16317. doi: 10.1002/chem.202001470. Epub 2020 Nov 09.

Herein, the design, synthesis, optical properties, and mechanofluorochromism characteristics of a series of conjugates having covalently linked triarylborane (TAB) and anil/boranil units (TAB-anil: 1 a-3 a and TAB-boranil: 1-3) are reported. The electronic interactions between TAB and anil/boranil in...

Cite
Nandi RP, Sudhakar P, Kalluvettukuzhy NK, et al. Triarylborane-Appended Anils and Boranils: Solid-State Emission, Mechanofluorochromism, and Phosphorescence. Chemistry. 2020;26(69):16306-16317doi: 10.1002/chem.202001470.
Nandi, R. P., Sudhakar, P., Kalluvettukuzhy, N. K., & Thilagar, P. (2020). Triarylborane-Appended Anils and Boranils: Solid-State Emission, Mechanofluorochromism, and Phosphorescence. Chemistry (Weinheim an der Bergstrasse, Germany), 26(69), 16306-16317. https://doi.org/10.1002/chem.202001470
Nandi, Rajendra Prasad, et al. "Triarylborane-Appended Anils and Boranils: Solid-State Emission, Mechanofluorochromism, and Phosphorescence." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 26,69 (2020): 16306-16317. doi: https://doi.org/10.1002/chem.202001470
Nandi RP, Sudhakar P, Kalluvettukuzhy NK, Thilagar P. Triarylborane-Appended Anils and Boranils: Solid-State Emission, Mechanofluorochromism, and Phosphorescence. Chemistry. 2020 Dec 09;26(69):16306-16317. doi: 10.1002/chem.202001470. Epub 2020 Nov 09. PMID: 32578898.
Copy Download .nbib Format: NLM
Chitosan from crustacean shell waste and its protective role against lead toxicity in .

Toxicology reports

Thilagar G, Samuthirapandian R.
PMID: 32071883
Toxicol Rep. 2020 Feb 08;7:296-303. doi: 10.1016/j.toxrep.2020.02.006. eCollection 2020.

In the current study heavy metal removing capability and antioxidant properties of chitosan supplemented diet tested in lead poisoning induced

Cite
Thilagar G, Samuthirapandian R. Chitosan from crustacean shell waste and its protective role against lead toxicity in . Toxicol Rep. 2020;7:296-303doi: 10.1016/j.toxrep.2020.02.006.
Thilagar, G., & Samuthirapandian, R. (2020). Chitosan from crustacean shell waste and its protective role against lead toxicity in . Toxicology reports, 7296-303. https://doi.org/10.1016/j.toxrep.2020.02.006
Thilagar, Gobinath, and Samuthirapandian, Ravichandran. "Chitosan from crustacean shell waste and its protective role against lead toxicity in ." Toxicology reports vol. 7 (2020): 296-303. doi: https://doi.org/10.1016/j.toxrep.2020.02.006
Thilagar G, Samuthirapandian R. Chitosan from crustacean shell waste and its protective role against lead toxicity in . Toxicol Rep. 2020 Feb 08;7:296-303. doi: 10.1016/j.toxrep.2020.02.006. eCollection 2020. PMID: 32071883; PMCID: PMC7016161.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 79 entries