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		<h1>Lĩnh vực và công trình nghiên cứu</h1>
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			<li>Thứ tư - 16/05/2018 05:16</li>
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			Lĩnh vực và công trình nghiên cứu chính
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			<span style="font-size:13pt"><span style="line-height:150%"><span style="font-family:&#039;Times New Roman&#039;,serif"><span style="line-height:150%">1. Điều chế porphyrin và tính chất quang phổ của porphyri</span></span></span></span>
<div style="text-align:center"><img alt="2" height="269" src="https://khoalyhoa.ued.udn.vn/uploads/nghien-cuu-khoa-hoc/2018_05/2.jpg" width="400" /></div>
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<span style="font-size:13pt"><span style="line-height:150%"><span style="font-family:&#039;Times New Roman&#039;,serif"><span style="line-height:150%">2. Điều chế hợp chất phát huỳnh quang BODIPY và tìm hiểu ứng dụng BODIPY trong khoa học y sinh</span></span></span></span>

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			<div style="text-align:center"><img alt="hh002" height="97" src="https://khoalyhoa.ued.udn.vn/uploads/nghien-cuu-khoa-hoc/2018_05/hh002.jpg" width="138" /></div>
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			<div style="text-align:center"><img alt="3" height="165" src="https://khoalyhoa.ued.udn.vn/uploads/nghien-cuu-khoa-hoc/2018_05/3.jpg" width="282" /></div>
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<span style="font-size:13pt"><span style="line-height:150%"><span style="font-family:&#039;Times New Roman&#039;,serif"><span style="line-height:150%">3. Điều chế các dẫn xuất của 2-pyrrolidinone dựa vào phản ứng nhiều thành phần (multi-component reaction) và đánh giá hoạt tính sinh học của chúng</span></span></span></span>

<div style="text-align:center"><img alt="hh001" height="323" src="https://khoalyhoa.ued.udn.vn/uploads/nghien-cuu-khoa-hoc/2018_05/hh001.jpg" width="527" /></div>
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<span style="font-size:13pt"><span style="line-height:150%"><span style="font-family:&#039;Times New Roman&#039;,serif"><span lang="VI" style="line-height:150%"><span style="font-family:&#039;Calibri&#039;,sans-serif"><img alt="" src="https://khoalyhoa.ued.udn.vn/file:///C:/Users/ADMINI~1.MAY/AppData/Local/Temp/msohtmlclip1/01/clip_image007.png" style="width:527px; height:310px" /></span></span></span></span></span><br  />
<span style="font-size:13pt"><span style="line-height:150%"><span style="font-family:&#039;Times New Roman&#039;,serif"><span style="line-height:150%">4. Nghiên cứu tổng hợp một số&nbsp; dẫn xuất&nbsp; 1,2,3-triazole thế ở vị trí 1,5</span></span></span></span><br  />
<span style="font-size:13pt"><span style="line-height:150%"><span style="font-family:&#039;Times New Roman&#039;,serif"><span style="line-height:150%">5. Nghiên cứu tổng hợp một số dẫn xuất NH-1,2,3-triazole</span></span></span></span><br  />
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<span style="color:rgb(192, 57, 43);"><strong><span style="font-size:13pt"><span style="line-height:150%"><span style="font-family:&#039;Times New Roman&#039;,serif"><span style="line-height:150%">Một số bài báo đã công bố</span></span></span></span></strong></span>

<ul>
	<li style="text-align: justify;"><span style="font-size:13pt"><span style="line-height:150%"><span style="tab-stops:182.45pt 267.45pt 399.6pt 470.45pt 538.9pt"><span style="font-family:&#039;Times New Roman&#039;,serif"><span style="line-height:150%">1. <b><u>N. T. Nguyen</u></b>, G Mamardashvili, M. Gruzdev, N. Mamardashvili and W. Dehaen, <sup>“</sup>Binding ability of Zn-tetraarylporphyrins with two, four and eight 4-(4-(3,6-bis(t-butyl)carbazol-9-ylphenyl)-1,2,3-4 triazole end groups towards N-containing substrates of different nature<sup>”</sup>, <i>Supramol. Chem</i>.</span> <b><span style="line-height:150%">25</span></b><span style="line-height:150%">, 180-188 (2013).</span></span></span></span></span></li>
	<li style="text-align: justify;"><span style="font-size:13pt"><span style="line-height:150%"><span style="tab-stops:182.45pt 267.45pt 399.6pt 470.45pt 538.9pt"><span style="font-family:&#039;Times New Roman&#039;,serif"><span style="line-height:150%">2. &nbsp;<b><u>N. T. Nguyen</u></b>, G. Mamardashvili, O. M. Kulikova, I. G. Scheblykin, N. Mamardashvili and W. Dehaen, <sup>“</sup>Binding ability of first and second generation / carbazolylphenyl dendrimers with Zn(II) tetraphenylporphyrin core towards small heterocyclic substrates<sup>”</sup>, <i>RSC Adv</i>.</span> <b><span style="line-height:150%">4</span></b><span style="line-height:150%">, 19703-19709 (2014).</span></span></span></span></span></li>
	<li style="text-align: justify;"><span style="font-size:13pt"><span style="line-height:150%"><span style="tab-stops:182.45pt 267.45pt 399.6pt 470.45pt 538.9pt"><span style="font-family:&#039;Times New Roman&#039;,serif"><span style="line-height:150%">3. <b><u>N. T. Nguyen</u></b>, E. Coutiño, J. Hofkens, I. Scheblykin, W. Dehaen and M. Kruk<i>, <sup>“</sup></i>Porphyrin core dendrimers with ether-linked carbazole dendrons: dual luminescence of core and conformational flexibility of dendritic shell<sup>”</sup>, <i>Macroheterocycles</i> <b>7</b>, 240-248 (2014).</span></span></span></span></span></li>
	<li style="text-align: justify;"><span style="font-size:13pt"><span style="line-height:150%"><span style="tab-stops:182.45pt 267.45pt 399.6pt 470.45pt 538.9pt"><span style="font-family:&#039;Times New Roman&#039;,serif"><span style="line-height:150%">4. <b><u>N. T. Nguyen</u></b>, J. Hofkens, I. Scheblykin, M. Kruk and W. Dehaen, <sup>“</sup>Click Reaction Synthesis and Photophysical Studies of New Dendritic Metalloporphyrins<sup>”</sup>, <i>Eur. J. Org. Chem</i>. <b>8</b>, 1766–1777 (2014).</span></span></span></span></span></li>
	<li style="text-align: justify;"><span style="font-size:13.0pt"><span style="line-height:115%"><span style="font-family:&#039;Times New Roman&#039;,serif">5. <b><u>N. T. Nguyen</u></b>, B. Verbelen, V. Leen, E. Waelkens, W. Dehaen and M. Kruk, <sup>“</sup>Excitation energy deactivation funnel in 3-substituted BODIPY-porphyrin conjugate<sup>”</sup>, <i>Journal of Luminescence</i> <b>179</b>, 306-313 (2016).</span></span></span></li>
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