A triphenylamine terpyridine manganese complex having double functions including two-photon development and magnetic resonance development and a synthetic method thereof

A technology of manganese terpyridine and magnetic resonance, applied in organic chemistry, particle and sedimentation analysis, analysis of materials, etc., can solve the problem of low sensitivity, and achieve the effect of low excitation energy, low cost, and enhanced magnetic resonance signal

Active Publication Date: 2017-03-15
ANHUI UNIVERSITY
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  • A triphenylamine terpyridine manganese complex having double functions including two-photon development and magnetic resonance development and a synthetic method thereof
  • A triphenylamine terpyridine manganese complex having double functions including two-photon development and magnetic resonance development and a synthetic method thereof
  • A triphenylamine terpyridine manganese complex having double functions including two-photon development and magnetic resonance development and a synthetic method thereof

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[0041] Example 1:

[0042] take ligand L 1 (0.202g, 0.400mmol) was dissolved in 20mL of absolute ethanol and placed in a 50mL round-bottomed flask, added containing Mn(OAc) 2 ·4H 2 O (0.049g, 0.200mmol) in 20mL ethanol solution, heated to reflux for 4h, after the reaction was completed, the reaction solution was cooled to room temperature, and then NH was added to the reaction solution 4 PF 6 (0.082g, 0.500mmol), continue to heat to reflux for 2h to precipitate a red solid, filter while hot, filter under reduced pressure to collect the filter cake, recrystallize with absolute ethanol to obtain the target product Mn10.206g, a red solid, yield 75.90% (calculated according to the amount of ligand, the same below).

[0043] M.P.: 232℃. 1 H NMR (400MHz, d 6 -DMSO,ppm): δ8.72(d,J=31.1Hz,12H),8.04(s,4H),7.86(s,4H),7.52(s,4H),7.34(s,8H),7.11( s,14H),5.15(s,2H),4.49(s,4H).IR(cm -1): 3421(m), 3063(m), 2922(m), 1587(vs), 1512(s), 1475(s), 1417(m), 1329(s), 1288(m), 1196(s) ), 10...

Example Embodiment

[0044] Example 2:

[0045] take ligand L 2 (0.214 g, 0.400 mmol) was dissolved in 20 mL of absolute ethanol and placed in a 50 mL round-bottomed flask, added containing Mn(OAc) 2 ·4H 2 O (0.049g, 0.200mmol) in 20mL ethanol solution, heated to reflux for 4h, after the reaction was completed, the reaction solution was cooled to room temperature, and then NH was added to the reaction solution 4 PF 6 (0.082g, 0.500mmol), continue to heat to reflux for 2h to precipitate a red solid, filter while hot, filter under reduced pressure to collect the filter cake, recrystallize with absolute ethanol to obtain the target product Mn20.211g, a red solid, yield 74.45% (calculated according to the amount of ligand, the same below).

[0046] M.P.: 236℃. 1 H NMR (400MHz, d 6 -DMSO,ppm): δ8.72(d,J=30.9Hz,12H),8.03(s,4H),7.85(s,4H),7.52(s,4H),7.32(s,8H),7.09( s,13H),5.15(s,4H),4.49(s,8H).IR(cm -1 ): 3393(m), 3063(m), 2922(m), 2872(m), 1593(vs), 1510(s), 1475(s), 1417(m), 1327(s), 1288(m )...

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Abstract

A triphenylamine terpyridine manganese complex having double functions including two-photon development and magnetic resonance development and a synthetic method thereof are disclosed. The structure formula of the complex is shown in the description. The complex has a two-photon development function and a magnetic resonance development function, and can be adopted as a contrast medium for double modes. Compared with a commercial nuclear magnetic contrast medium that is Gd-DTPA, the complex can be ingested by cells well so that magnetic resonance signals are enhanced.

Description

technical field [0001] The invention relates to a triphenylamine terpyridine manganese complex with dual functions of two-photon imaging and magnetic resonance imaging and a synthesis method thereof, which can be applied to the dual-mode imaging functions of two-photon microscopic imaging and magnetic resonance imaging of living cells in biology. It has obvious commercial application value. Background technique [0002] Magnetic resonance imaging (MRI) is a relatively new medical imaging technique, and it is attracting more and more attention for medical diagnosis. In 1945, two research groups headed by E.M.Purcell of Harvard University and F.Bloch of Stanford University observed the phenomenon of nuclear magnetic resonance almost simultaneously, and they both won the 1952 Nobel Prize in Physics. In 1953, Varian Corporation of the United States successfully developed the world's first commercial nuclear magnetic resonance instrument. As research on contrast agents has deve...

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Application Information

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IPC IPC(8): C07D213/38G01N15/10
CPCC07D213/38G01N15/10G01N2015/1006
Inventor 田玉鹏史亚南肖陆飞田肖和李飞吴大俊杜威周虹屏李胜利吴杰颖
Owner ANHUI UNIVERSITY
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