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<title>Volume:3 Number:1 December 2015</title>
<link>http://repository.rjt.ac.lk/handle/123456789/17</link>
<description/>
<pubDate>Sat, 11 Apr 2026 12:18:38 GMT</pubDate>
<dc:date>2026-04-11T12:18:38Z</dc:date>
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<title>Morphometric and DNA Fingerprinting Strategies for the Detection of Rice Flour Adulteration in Chili Powder</title>
<link>http://repository.rjt.ac.lk/handle/123456789/4427</link>
<description>Morphometric and DNA Fingerprinting Strategies for the Detection of Rice Flour Adulteration in Chili Powder
Chamikara, M.D.M.; Ishan, M.; Dissanayake, D.R.R.P.; Sooriyapathirana, S.D.S.S.
</description>
<pubDate>Tue, 01 Dec 2015 00:00:00 GMT</pubDate>
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<dc:date>2015-12-01T00:00:00Z</dc:date>
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<title>Entrepreneurial Strategies Adopted by Rural Business Operators in Sri Lanka</title>
<link>http://repository.rjt.ac.lk/handle/123456789/4426</link>
<description>Entrepreneurial Strategies Adopted by Rural Business Operators in Sri Lanka
Navarathne, K.A.S.
</description>
<pubDate>Tue, 01 Dec 2015 00:00:00 GMT</pubDate>
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<dc:date>2015-12-01T00:00:00Z</dc:date>
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<title>Comparison of Yield, Nutritive Value and Silage Quality of Fodder Sorghum (Soghum bicolor) and Maize (Zea mays)with Hibrid Napier Variety CO-3</title>
<link>http://repository.rjt.ac.lk/handle/123456789/36</link>
<description>Comparison of Yield, Nutritive Value and Silage Quality of Fodder Sorghum (Soghum bicolor) and Maize (Zea mays)with Hibrid Napier Variety CO-3
Bandara, P.G.G.; Premalal, G.C.C.; Nayananjalie, W.A.D.
</description>
<pubDate>Thu, 01 Dec 2016 00:00:00 GMT</pubDate>
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<dc:date>2016-12-01T00:00:00Z</dc:date>
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<title>Synthesis of Phenanthroline-Based Polyphenylenes via a Diels-Alder Cycloaddition Reaction</title>
<link>http://repository.rjt.ac.lk/handle/123456789/35</link>
<description>Synthesis of Phenanthroline-Based Polyphenylenes via a Diels-Alder Cycloaddition Reaction
Lankage, Buddhie  S.; Perera, S.D.; Draper, S.M.
Abstract&#13;
Conjugated polyarenes have been the focus of considerable interest due to their&#13;
potential for serving as materials for electroluminescence devices, since they possess&#13;
high fluorescence efficiency and are technically processable. A novel Family of&#13;
phenanthroline-based compounds were synthesised via a [2+4] Diels-Alder&#13;
cycloaddition reaction between specifically designed cyclopentadienone based&#13;
synthons that incorporate the already fused phenanthroline moiety 11b-Hydroxy-1,3-&#13;
diphenyl-1,11b-dihydro-7,8-diaza-cyclophenta[l]phenanthrene-2-one (1a) and 11b-&#13;
Hy d r o x y - 1 , 3 - d i ( 4 - t e r t - b u t y l p h e n y l ) - 1 , 1 1 b - d i h y d r o - 7 , 8 - d i a z a -&#13;
cyclophenta[l]phenanthrene-2-one (1b) and various di-substituted acetylenes. These&#13;
systems have been found to display tuneable fluorescent capabilities, which make them&#13;
promising material for application in optoelectronics as well showing excellent metal&#13;
coordination potential
</description>
<pubDate>Tue, 01 Dec 2015 00:00:00 GMT</pubDate>
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<dc:date>2015-12-01T00:00:00Z</dc:date>
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