{"id":1474,"date":"2018-01-29T14:43:46","date_gmt":"2018-01-29T07:43:46","guid":{"rendered":"https:\/\/www.chemistry.su.ac.th\/?p=1474"},"modified":"2026-02-27T16:50:41","modified_gmt":"2026-02-27T09:50:41","slug":"%e0%b8%ad%e0%b8%b2%e0%b8%88%e0%b8%b2%e0%b8%a3%e0%b8%a2%e0%b9%8c-%e0%b8%94%e0%b8%a3-%e0%b8%88%e0%b8%b4%e0%b8%95%e0%b8%99%e0%b8%a0%e0%b8%b2-%e0%b8%a8%e0%b8%b4%e0%b8%a3%e0%b8%b4%e0%b8%a3%e0%b8%b1","status":"publish","type":"post","link":"https:\/\/chem.sc.su.ac.th\/?p=1474","title":{"rendered":"\u0e1c\u0e39\u0e49\u0e0a\u0e48\u0e27\u0e22\u0e28\u0e32\u0e2a\u0e15\u0e23\u0e32\u0e08\u0e32\u0e23\u0e22\u0e4c \u0e14\u0e23.\u0e08\u0e34\u0e15\u0e19\u0e20\u0e32 \u0e28\u0e34\u0e23\u0e34\u0e23\u0e31\u0e01\u0e29\u0e4c"},"content":{"rendered":"
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\u0e2d\u0e35\u0e40\u0e21\u0e25\u0e4c:<\/span> jitnapasirirak@gmail.com, sirirak_j@silpakorn.edu<\/h4>\n

\u0e2b\u0e49\u0e2d\u0e07\u0e1e\u0e31\u0e01:<\/span> 4210\/4 Science Building 4<\/h4>\n

\u0e42\u0e17\u0e23:<\/span> 034-109686 ext. 207316<\/h4>\n

\u0e40\u0e27\u0e47\u0e1a\u0e44\u0e0b\u0e15\u0e4c:<\/span> -<\/h4>\n

\u0e01\u0e32\u0e23\u0e28\u0e36\u0e01\u0e29\u0e32:<\/span><\/h3>\n

Ph.D. (Chemistry) University of Bristol, UK (2011)<\/h4>\n

MSci (Chemistry) University of Bristol, UK (2007)<\/h4>\n<\/div>\n<\/div><\/div><\/div><\/div>
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\u0e07\u0e32\u0e19\u0e27\u0e34\u0e08\u0e31\u0e22\u0e17\u0e35\u0e48\u0e2a\u0e19\u0e43\u0e08<\/strong>:<\/span><\/h2>\n

Molecular modelling, Natural dye and Lake pigment<\/h3>\n

\u0e1c\u0e25\u0e07\u0e32\u0e19\u0e15\u0e35\u0e1e\u0e34\u0e21\u0e1e\u0e4c<\/strong>:<\/span><\/h2>\n
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    Oekchuae, S., Sirirak<\/strong>, J<\/strong>.<\/span>, Charoensuksai, P., Wongprayoon, P., Chuaypen, N., Boonsombat, J., Ruchirawat, S., Tangkijvanich, P., Suksamrarn, A., Limpachayaporn, P. (2022). \u201cThe Design and Synthesis of a New Series of 1,2,3-Triazole-Cored Structures Tethering Aryl Urea and Their Highly Selective Cytotoxicity toward HepG2.\u201d Pharmaceuticals,<\/strong><\/span> 15: 504. (Scopus)<\/h4>\n<\/li>\n
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    Limpachayaporn, P., Nuchpun, S., Sirirak<\/strong>,<\/span>, Charoensuksai, P., Wongprayoon, P., Chuaypen, N., Tangkijvanich, P., Suksamrarn, A. (2022). \u201cmeta-Ureidophenoxy-1,2,3-triazole hybrid as a novel scaffold for promising HepG2 hepatocellular carcinoma inhibitors: Synthesis, biological evaluation and molecular docking studies.\u201d Bioorganic & Medicinal Chemistry,<\/strong><\/span> 74: 117048. (ISI)<\/h4>\n<\/li>\n
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    Vicharn, S., Sirirak<\/strong>, J<\/strong>.<\/span>, Phutdhawong, W., Taechowisan, T., Phutdhawong, W.S. (2022). \u201cSynthesis of 2-substituted indoles and evaluation of their antibacterial activity and inhibitory effects on the efflux pump of methicillin-resistant Staphylococcus aureu.s\u201d Journal of Applied Pharmaceutical Science,<\/strong><\/span> 12, 1: 084-093. (Scopus)<\/h4>\n<\/li>\n
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    Petdum A., Kaewnok N., Panchan W., Charoenpanich A., Sirirak J.<\/strong><\/span>, Sahasithiwat S., Sooksimuang T., Wanichacheva N. (2022). \u201cNovel rapid \u201cturn on\u201d tetrahydro-[5]helicene-based fluorescence sensor for selective detection of Cd2+ with a remarkable large Stokes shift and its applications in food samples and living cell.\u201d Journal of Photochemistry and Photobiology A: Chemistry,<\/strong><\/span> 423: 113578. (ISI, SCOPUS)<\/h4>\n<\/li>\n
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    Keeratichamroen S., Lirdprapamongkol K., Thongnest S., Boonsombat J., Chawengrum P., Sornprachum T., Sirirak, J.<\/span>,<\/strong> Verathamjamras C., Ornnork N., Ruchirawat S., Svasti J. (2022). \u201cJAK2\/STAT3-mediated dose-dependent cytostatic and cytotoxic effects of sesquiterpene lactones from Gymnanthemum extensum on A549 human lung carcinoma cells.\u201d Oncology Reports,<\/strong><\/span> 47(1): 1-11. (SCOPUS)<\/h4>\n<\/li>\n
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    Leerawatthanakun S., Charoenwongpaiboon T., Klaewkla M., Chunsrivirot S., Sirirak, J.<\/span>,<\/strong> Sriwitool T.-E., Wangpaiboon K., Pichyangkura R. (2022). \u201cHigh surfactant-tolerant \u03b2-mannanase isolated from Dynastes hercules larvae excrement, and identification of its hotspot using site-directed mutagenesis and molecular dynamics simulations.\u201d Enzyme and Microbial Technology,<\/strong><\/span> 154: 109956.<\/h4>\n<\/li>\n
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    Chuenbarn T., Sirirak, J.<\/span>,<\/strong> Tuntarawongsa S., Okonogi S., Phaechamud, T. (2022). \u201cDesign and Comparative Evaluation of Vancomycin HCl-Loaded Rosin-Based In Situ Forming Gel and Microparticles.\u201d Gels,<\/strong><\/span> 8(4): 231. (Scopus)<\/h4>\n<\/li>\n
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    Petdum, A., Sirirak, J.<\/span>,<\/strong> Lee, V. S., Nienaber, H. A., Panchan, W., Sooksimuang, T., Wanichacheva, N. (2020). \u201cNew [5]helicene derivatives with large stokes shifts for Hg2+<\/sup> determination and their application in drinking water, river water and tuna fillet.\u201d Science, Engineering and Health Studies<\/strong>,<\/span> 14(1): 32-46.<\/h4>\n<\/li>\n
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    Sirirak,<\/strong><\/span> ,<\/strong> Worawannotai, N., Suwanchawalit, C., Chayabutra, S. (2020). \u201cPreparation and characterization of lake pigments from sappan wood using Thai local clays.\u201d Journal of Metals, Materials and Minerals,<\/strong><\/span> 30(1): 20-28.<\/h4>\n<\/li>\n
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    Sasiwimon, K., Panchan, W., Charoenpanich, A., Sirirak,<\/strong><\/span> , <\/strong>Sahasithiwat, S., Swanglap, P., Promarak, V., Panchan, W., Charoenpanich, A., Sirirak, J., Sahasithiwat, S., Swanglap, P., Promarak, V., Thamyongkit, P., Wanichacheva, N. (2020) \u201cA method to detect Hg2+<\/sup> in vegetable via a \u201cTurn\u2013ON\u201d Hg2+<\/sup>\u2013Fluorescent sensor with a nanomolar sensitivity.\u201d Journal of Photochemistry and Photobiology A: Chemistry,<\/strong><\/span> 389: 112224.<\/h4>\n<\/li>\n
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    Petdum, A., Faichu, N., Sirirak,<\/strong><\/span> ,<\/strong> Khammultri, P., Promarak, V., Panchan, W., Sooksimuang, T., Charoenpanich, A., Wanichacheva, N. (2020). \u201c[5]Helicene-rhodamine 6 G hybrid-based sensor for ultrasensitive Hg2+ detection and its biological applications.\u201d Journal of Photochemistry and Photobiology A: Chemistry,<\/span><\/strong> 394: 112473.<\/h4>\n<\/li>\n
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    Petdum, A., Waraeksiri, N., Hanmeng, O., Jarutikorn, S., Chaneam, S., Sirirak<\/strong>,<\/span> ,<\/strong> Charoenpanich, A., Panchan, W., Sooksimuang, T., Wanichacheva, N., (2020). \u201cA new water-soluble Fe3+<\/sup> fluorescence sensor with a large Stokes shift based on [5]helicene derivative: Its application in flow injection analysis and biological systems.\u201d\u00a0 Journal of Photochemistry and Photobiology A: Chemistry,<\/strong><\/span> 401: 112769.<\/h4>\n<\/li>\n
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    Hanmeng, O., Chailek, N., Charoenpanich, A., Phuekvilai, P., Yookongkaew, N., Sanmanee, N., Sirirak<\/strong>,<\/span> , <\/strong>Swanglap, P., Wanichacheva, N. (2020). \u201cCu2+<\/sup>-selective NIR fluorescence sensor based on heptamethine cyanine in aqueous media and its application.\u201d Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy,<\/span><\/strong> 240: 118606.<\/h4>\n<\/li>\n
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    \u0e0a\u0e13\u0e34\u0e20\u0e23\u0e13\u0e4c \u0e27\u0e14\u0e35\u0e28\u0e34\u0e23\u0e34\u0e28\u0e31\u0e01\u0e14\u0e34\u0e4c, \u0e2a\u0e38\u0e1e\u0e23\u0e23\u0e13\u0e35 \u0e09\u0e32\u0e22\u0e30\u0e1a\u0e38\u0e15\u0e23 \u0e41\u0e25\u0e30\u0e08\u0e34\u0e15\u0e19\u0e20\u0e32 \u0e28\u0e34\u0e23\u0e34\u0e23\u0e31\u0e01\u0e29\u0e4c<\/strong>,<\/span> (2563). \u201c\u0e1c\u0e25\u0e02\u0e2d\u0e07\u0e2a\u0e32\u0e22\u0e1e\u0e31\u0e19\u0e18\u0e38\u0e4c\u0e41\u0e25\u0e30\u0e27\u0e34\u0e18\u0e35\u0e01\u0e32\u0e23\u0e40\u0e15\u0e23\u0e35\u0e22\u0e21\u0e43\u0e1a\u0e21\u0e30\u0e21\u0e48\u0e27\u0e07\u0e17\u0e35\u0e48\u0e21\u0e35\u0e15\u0e48\u0e2d\u0e1c\u0e07\u0e2a\u0e35\u0e18\u0e23\u0e23\u0e21\u0e0a\u0e32\u0e15\u0e34\u0e08\u0e32\u0e01\u0e43\u0e1a\u0e21\u0e30\u0e21\u0e48\u0e27\u0e07\u0e17\u0e35\u0e48\u0e15\u0e23\u0e35\u0e22\u0e21\u0e14\u0e49\u0e27\u0e22\u0e27\u0e34\u0e18\u0e35\u0e01\u0e32\u0e23\u0e14\u0e39\u0e14\u0e0b\u0e31\u0e1a.\u201d \u0e27\u0e32\u0e23\u0e2a\u0e32\u0e23\u0e27\u0e34\u0e17\u0e22\u0e32\u0e28\u0e32\u0e2a\u0e15\u0e23\u0e4c\u0e1a\u0e39\u0e23\u0e1e\u0e32<\/strong>,<\/strong><\/span> 25(2): 545-562.<\/h4>\n<\/li>\n
  • \n

    \u0e1e\u0e25\u0e2d\u0e22\u0e1e\u0e31\u0e17\u0e18\u0e4c \u0e28\u0e38\u0e20\u0e23\u0e31\u0e15\u0e19\u0e4c\u0e18\u0e31\u0e0d\u0e0d\u0e32, \u0e20\u0e32\u0e19\u0e38\u0e1e\u0e31\u0e19\u0e18\u0e4c \u0e25\u0e34\u0e21\u0e1b\u0e0a\u0e22\u0e32\u0e1e\u0e23, \u0e2a\u0e38\u0e21\u0e19\u0e21\u0e32\u0e25\u0e22\u0e4c \u0e08\u0e31\u0e19\u0e17\u0e23\u0e4c\u0e40\u0e2d\u0e35\u0e48\u0e22\u0e21, \u0e2a\u0e38\u0e1e\u0e23\u0e23\u0e13\u0e35 \u0e09\u0e32\u0e22\u0e30\u0e1a\u0e38\u0e15\u0e23 \u0e41\u0e25\u0e30\u0e08\u0e34\u0e15\u0e19\u0e20\u0e32 \u0e28\u0e34\u0e23\u0e34\u0e23\u0e31\u0e01\u0e29\u0e4c<\/strong><\/span> (2562). \u201c\u0e01\u0e32\u0e23\u0e28\u0e36\u0e01\u0e29\u0e32\u0e08\u0e25\u0e19\u0e28\u0e32\u0e2a\u0e15\u0e23\u0e4c\u0e41\u0e25\u0e30\u0e44\u0e2d\u0e42\u0e0b\u0e40\u0e17\u0e2d\u0e21\u0e02\u0e2d\u0e07\u0e01\u0e32\u0e23\u0e14\u0e39\u0e14\u0e0b\u0e31\u0e1a\u0e1a\u0e23\u0e32\u0e0b\u0e34\u0e25\u0e35\u0e19\u0e08\u0e32\u0e01\u0e1d\u0e32\u0e07\u0e14\u0e49\u0e27\u0e22\u0e21\u0e2d\u0e19\u0e15\u0e4c\u0e21\u0e2d\u0e23\u0e34\u0e25\u0e42\u0e25\u0e44\u0e19\u0e17\u0e4c.\u201d \u0e27\u0e32\u0e23\u0e2a\u0e32\u0e23\u0e27\u0e34\u0e17\u0e22\u0e32\u0e28\u0e32\u0e2a\u0e15\u0e23\u0e4c\u0e41\u0e25\u0e30\u0e40\u0e17\u0e04\u0e42\u0e19\u0e42\u0e25\u0e22\u0e35 \u0e21\u0e2b\u0e32\u0e27\u0e34\u0e17\u0e22\u0e32\u0e25\u0e31\u0e22\u0e18\u0e23\u0e23\u0e21\u0e28\u0e32\u0e2a\u0e15\u0e23\u0e4c<\/strong>,<\/strong><\/span> 27(6): 989-1001.<\/h4>\n<\/li>\n
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    Praikaew, P., Maniam, S., Charoenpanich, A., Sirirak, J.<\/strong><\/span>, Promarak, V., Langford, S.J. and Wanichacheva, N. (2019). \u201cWater-soluble Cu2+- fluorescent sensor based on core-substituted naphthalene diimide and its application in drinking water analysis and live cell imaging.\u201d Journal of Photochemistry and Photobiology A: Chemistry,<\/strong> <\/span>382(1): 111852.<\/h4>\n<\/li>\n
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    Petdum, A., Sooksimuang, T., Wanichacheva, N., Sirirak, J.<\/strong><\/span> (2019). \u201cNatural colorimetric sensor from sappanwood for turn\u2013on selective Fe2+ detection in aqueous media and its application in water and pharmaceutical samples.\u201d Chemistry Letters,<\/strong><\/span> 48(7): 678-681. (ISI\/SCOPUS)<\/h4>\n<\/li>\n
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    Piyanuch, P., Sirirak, J.<\/strong><\/span>, Kamkaew, A., Weeranantanapa, O., Promarak, V., Burgess, K., Wanichacheva, N. (2019). \u201cNear\u2010Infrared fluorescence chemosensor based on isothiocyanate\u2010aza\u2010BODIPY for cyanide detection in ppb level: Applications in buffer media and living cell imaging.\u201d ChemPlusChem,<\/strong><\/span> 84(3): 252-259 (ISI\/SCOPUS)<\/h4>\n<\/li>\n
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    Rattanopas, S., Piyanuch, P., Wisansin, K., Charoenpanich, A., Sirirak, J.<\/strong><\/span>, Phutdhawong, W.S., Wanichacheva, N. (2019). \u201cIndole-based fluorescent sensors for selective sensing of Fe2+<\/sup> and Fe3+<\/sup> in aqueous buffer systems and their applications in living cells.\u201d Journal of Photochemistry and Photobiology A-Chemistry,<\/strong><\/span> 377: 138-148 (ISI\/SCOPUS)<\/h4>\n<\/li>\n
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    Jarutikorn, S., Kraithong, S., Sirirak, J.<\/strong><\/span>, Panchan, W., Sooksimuang, T., Charoenpanich, A. Wanichacheva, N. (2019). \u201cEnvironmentally Friendly Ag+ Detection of \u201cTurn-on\u201d Fluorescent Sensor with a Mega-Stokes Shift and Its Application in Biological Systems.\u201d Oriental Journal of Chemistry,<\/strong><\/span> 35(3): 1227-1234. (ISI)<\/h4>\n<\/li>\n
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    Phutdhawong, W., Rattanopas, S., Sirirak, J.<\/span>,<\/strong> Taechowisan, T., Phutdhawong, W.S. (2019). \u201cSynthesis and Anticancer Activity Evaluation of Azepinobisindoles; The Isomeric Iheyamine A-derivatives.\u201d Oriental Journal of Chemistry,<\/strong><\/span> 35(2): 723-731. (ISI)<\/h4>\n<\/li>\n
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    Sukaram, T., Sirisakwisut, P., Sirirak, J.<\/span>, <\/strong>Nacapricha, D., Chaneam, S. (2018). \u201cEnvironmentally friendly method for determination of ammonia nitrogen in fertilisers and wastewaters based on flow injection-spectrophotometric detection using natural reagent from orchid flower.\u201d International Journal of Environmental Analytical Chemistry,<\/strong><\/span> 98: 907-920.<\/h4>\n<\/li>\n
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    Sutinee Girdthep, Sirirak, J.<\/span>,<\/strong> Donraporn Daranarong, Rathawat Daengngern, Supanee Chayabutra. (2018). \u201cPhysico-chemical characterization of natural lake pigments obtained from Caesalpinia Sappan Linn. and their composite films for poly (lactic acid)-based packaging materials.\u201d Dyes and Pigments,<\/strong><\/span> 157: 27-39.<\/h4>\n<\/li>\n
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    Kraithong, S., Sangsuwan, R., Worawannotai, N., Sirirak, J.<\/span>, <\/strong>Charoenpanich, A., Thamyongkit, P., Wanichacheva, N. (2018). \u201cTriple detection modes for Hg2+sensing based on NBD-fluorescent and colorimetric sensor and its potential in cell imaging.\u201d New Journal of Chemistry,<\/strong><\/span> 42: 13180-13180.<\/h4>\n<\/li>\n
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    Sakunkaewkasem, S., Petdum , A., Waraporn Panchan, Sirirak, J.<\/span>, <\/strong>Charoenpanich, A., Sooksimuang, T., Wanichacheva., (2018). \u201cDual-analyte fluorescent sensor based on [5]helicene derivative with super large stokes shift for the selective determinations of Cu2+<\/sup> or Zn2+<\/sup> in Buffer Solutions and Its Application in Living Cell.\u201d ACS Sensors,<\/strong><\/span> 3 (5): 1016\u20131023.<\/h4>\n<\/li>\n
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    Kaewnok, N., Petdum, A., Sirirak, J.<\/span>, <\/strong>Charoenpanich, A., Panchan, W., Sahasithiwat, S., Sooksimuangc, T., Wanichacheva, N. (2018). \u201cNovel Cu2+-specific \u2018\u2018Turn-ON\u2019\u2019 fluorescent probe based on [5]helicene with very large Stokes shift and its potential application in living cells.\u201d New Journal of Chemistry<\/strong>.<\/span>, 42: 5540.<\/h4>\n<\/li>\n
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    Kraitong, S., Sirirak, J.<\/span>, <\/strong>Soisuwan, K., Wanichacheva, N., Swanglap, P. (2018). \u201cEnhancing sensitivity of novel Hg2+<\/sup> fluorescent sensor via plasmonic enhancement of silver nanoparticles.\u201d Sensors and Actuators<\/strong>, B: Chemical<\/strong>,<\/span> 258: 694-703.<\/h4>\n<\/li>\n
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    Petdum, A., Panchan, W., Swanglap, P., Sirirak, J.<\/span>, <\/strong>Sooksimuang, T., Wanichacheva, N. (2018). \u201c\"Turn-ON\" [5]helicene-based fluorescence sensor with very large Stokes shift for highly selective detection of Ag+<\/sup> and AgNPs.\u201d Sensors and Actuators<\/strong>, B: Chemical<\/strong>,<\/span> 259: 862 - 870.<\/h4>\n<\/li>\n
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    Puangsamlee, T., Tachapermpon, Y., Kammalun, P., Sukrat, K., Wainiphithapong, C., Sirirak, J.<\/span>, <\/strong>Wanichacheva, N. (2018). \u201cSolvent control bifunctional fluorescence probe for selective detection of Cu2+<\/sup> and Hg2+ <\/sup>via the excimer of pyrenylacetamide subunits.\u201d Journal of Luminescence<\/strong><\/span>, 196: 227 \u2013 235.<\/h4>\n<\/li>\n
  • \n

    Petdum, A., Panchan, W., Sirirak, J.<\/span>, <\/strong>Promarak, V., Sooksimuang, T., Wanichacheva, N. (2017). \u201cColorimetric and fluorescent sensing of a new FRET system via [5]helicene and rhodamine 6G for Hg2+<\/sup>\u201d Dalton Trans<\/strong>.<\/span>, 46: 16251\u201316256.<\/h4>\n<\/li>\n
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    Tachapermpon, Y., Thavornpradit, S., Charoenpanich, A., Sirirak, J.<\/span>, <\/strong>Burgess, K., Wanichacheva, N. (2017). \u201cNear-infrared aza-BODIPY \ufb02uorescent probe for selective Cu2+<\/sup> detection and its potential in living cell imaging.\u201d Dalton Trans<\/strong>.<\/span>, 46: 16251.<\/h4>\n<\/li>\n
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    Sirirak, J.<\/span>, <\/strong>Sertphon, D., Phonsri, W., Harding, P., Harding, D. J. (2017). \u201cComparison of density functionals for the study of the high spin low spin gap in Fe(III) spin crossover complexes\u201d Int J Quantum Chem<\/strong>.<\/span>, 117(9), e25362.<\/h4>\n<\/li>\n
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    Tachapermpon, Y., Chaneam, S., Charoenpanich, A., Sirirak, J.<\/span>, <\/strong>Wanichacheva, N. (2017). \u201cHighly Cu2+-sensitive and selective colorimetric and fluorescent probes: Utilizations in batch, flow analysis and living cell imaging.\u201d Sensors and Actuators B: Chemical<\/strong>,<\/span> 241: 868-878.<\/h4>\n<\/li>\n
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    Kraithong, S., Damrongsak, P., Suwatpipat, K., Sirirak, J.<\/span>,<\/strong> Swanglap, P., Wanichacheva. N. (2016). \u201cHighly Hg2+<\/sup>-sensitive and selective fluorescent sensors in aqueous solution and sensors-encapsulated polymeric membrane.\u201d RSC Adv<\/strong>.<\/span>, 6: 10401-10411<\/h4>\n<\/li>\n
  • \n

    Thavornpradit, S., Sirirak, J.<\/span>, <\/strong>Wanichacheva, N. (2016). \u201cTurn-on naphthalimide fluorescent sensor with high quantum yield and large Stokes shift for the determination of Cu(II).\u201d J Photochem Photobiol A Chem<\/strong>.<\/span>, 330: 55-63<\/h4>\n<\/li>\n
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    , Insiti, Jitthiang, P., Harding, P., Chainok, K., Chotima, R., Sirirak, J.<\/span>, <\/strong>Blackwood, S., Alka\u015f, A., Telfer, S. G., Harding, D. J. (2016). \u201cSubstituent modulated packing in octahedral Ni(II) complexes.\u201d Polyhedron,<\/strong><\/span> 114: 242-248<\/h4>\n<\/li>\n
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    Sirirak, J.<\/span>, <\/strong>Harding, D. J., Harding, P., Murray, K. S., Moubaraki, B., Liu, L., Telfer, S. G. (2015). \u201cSpin Crossover in cis Manganese (III) Quinolylsalicylaldiminates.\u201d Eur<\/strong>. J<\/strong>. Inor<\/strong>. Chem<\/strong><\/span>., 15, 2534-2542.<\/h4>\n<\/li>\n
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    Harding, D. J., Phonsri, W., Harding, P., Sirirak<\/strong>, J<\/strong>.<\/span>, Tangtirungrotechai, Y., Webster, R. D., Adams, H. (2014). \u201cCopper hydrotris(3,5-diphenylpyrazolyl)borate dithiocarbamates: attempting to model azurin\u201d New J<\/strong>. Chem<\/strong>.<\/span>, 39: 1489.<\/h4>\n<\/li>\n
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    Sirirak, J.<\/span>, <\/strong>Harding, D. J., Harding, P., Liu, L., Telfer, S. G. (2014). \u201cSolvatomorphism and electronic communication in FeIII N,N-bis(salicylidene)-1,3-propanediamine dimers.\u201d Aus<\/strong>. J<\/strong>. Chem<\/strong>.<\/span>, 68(5): 766-773.<\/h4>\n<\/li>\n
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    Kamp, M. W. v. d., Sirirak, J.<\/span>, <\/strong>\u017burek, J., Allemann. R. K., Mulholland, A. J. (2013). \u201cConformational Change and Ligand Binding in the Aristolochene Synthase Catalytic Cycle.\u201d Biochemistry<\/strong><\/span>, 52: 8094.<\/h4>\n<\/li>\n
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    Chudyk, E., Kazimierowicz, E. D., Langner, K. M., Sokalski, W. A., Lodola, A., Mor, M., Sirirak, J.<\/span>, <\/strong>Mulholland, A. J. (2013). \u201cNonempirical energetic analysis of reactivity and covalent inhibition of fatty acid amide hydrolase.\u201d J<\/strong>. Phys<\/strong>.Chem<\/strong>. B<\/strong>,<\/span> 117(22): 6656.<\/h4>\n<\/li>\n
  • \n

    Sirirak, J.<\/span>, <\/strong>Phonsri, W., Harding, D. J., Harding, P., Phommon, P., Chaoprasa, W., Hendry, R. M., Roseveare, T. M., Adams, H. (2013). \u201cHalogen substituted quinolylsalicylaldimines: Four halogens three structural types.\u201d J<\/strong>. Mol<\/strong>. Struct<\/strong>.<\/span>, 1036: 439.<\/h4>\n<\/li>\n<\/ul>\n<\/div>\n<\/div><\/div><\/div><\/div><\/div>","protected":false},"excerpt":{"rendered":"

    \u0e2d\u0e35\u0e40\u0e21\u0e25\u0e4c: jitnapasirirak@gmail.com, sirirak_j@silpakorn.edu \u0e2b\u0e49\u0e2d\u0e07\u0e1e\u0e31\u0e01: 4210\/4 Science Building 4 \u0e42\u0e17\u0e23: 034-109686 ext. 207316 \u0e40\u0e27\u0e47\u0e1a\u0e44\u0e0b\u0e15\u0e4c: – \u0e01\u0e32\u0e23\u0e28\u0e36\u0e01\u0e29\u0e32: Ph.D. (Chemistry) University of Bristol, UK (2011) MSci (Chemistry) University of Bristol, UK (2007) \u0e07\u0e32\u0e19\u0e27\u0e34\u0e08\u0e31\u0e22\u0e17\u0e35\u0e48\u0e2a\u0e19\u0e43\u0e08: Molecular modelling, Natural dye and Lake pigment \u0e1c\u0e25\u0e07\u0e32\u0e19\u0e15\u0e35\u0e1e\u0e34\u0e21\u0e1e\u0e4c: Oekchuae, S., Sirirak, J., Charoensuksai, P., Wongprayoon, P., Chuaypen, N., Boonsombat, J., Ruchirawat, S., Tangkijvanich, P., Suksamrarn, […]<\/p>\n","protected":false},"author":11,"featured_media":6660,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[46],"tags":[],"class_list":["post-1474","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-46"],"_links":{"self":[{"href":"https:\/\/chem.sc.su.ac.th\/index.php?rest_route=\/wp\/v2\/posts\/1474","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/chem.sc.su.ac.th\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/chem.sc.su.ac.th\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/chem.sc.su.ac.th\/index.php?rest_route=\/wp\/v2\/users\/11"}],"replies":[{"embeddable":true,"href":"https:\/\/chem.sc.su.ac.th\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1474"}],"version-history":[{"count":33,"href":"https:\/\/chem.sc.su.ac.th\/index.php?rest_route=\/wp\/v2\/posts\/1474\/revisions"}],"predecessor-version":[{"id":6816,"href":"https:\/\/chem.sc.su.ac.th\/index.php?rest_route=\/wp\/v2\/posts\/1474\/revisions\/6816"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/chem.sc.su.ac.th\/index.php?rest_route=\/wp\/v2\/media\/6660"}],"wp:attachment":[{"href":"https:\/\/chem.sc.su.ac.th\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1474"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/chem.sc.su.ac.th\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=1474"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/chem.sc.su.ac.th\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=1474"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}