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CAS No. : | 17252-51-6 | MDL No. : | MFCD00038046 |
Formula : | C13H14N2 | Boiling Point : | - |
Linear Structure Formula : | C5NH4CH2CH2CH2C5NH4 | InChI Key : | OGNCVVRIKNGJHQ-UHFFFAOYSA-N |
M.W : | 198.26 | Pubchem ID : | 87019 |
Synonyms : |
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Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P280-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302+H312+H332-H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
36% | In methanol; at 110℃; for 72h;High pressure; | 2.2.4 [Ni(PA)(bpp)(H2O)2]·DMF}n (4) (0007) A mixture of Ni(NO3)2·6H2O (0.291g, 1mmol), H2PA (0.388g, 1mmol), bpp (0.198g, 1mmol) and KOH (0.112g, 2mmol) in DMF?H2O?MeOH (1:2:2) (10mL) was heated for 72h at 110°C in a Teflon-lined stainless steel vessel (23mL). The reaction system was then cooled to room temperature and green block crystals of 4 were collected, washed with water and dried in air (yield 36percent). IR data (KBr, cm?1): 3381m, 3056w, 2931w, 2360m, 1647vs, 1616m, 1569s, 1509m, 1460m, 1401m, 1337s, 1270w, 1231w, 1155w, 1102w, 815m, 755m, 668w, 604w, 526w. Anal. Calc. for C39H39N3NiO9 (752.44): C, 62.20; H, 5.18; N, 5.58. Found: C, 62.27; H, 5.24; N, 5.53percent. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
38% | In water; N,N-dimethyl-formamide; at 110℃; for 72h;High pressure; | General procedure: 2.2.4 [Ni(PA)(bpp)(H2O)2]·DMF}n (4) (0007) A mixture of Ni(NO3)2·6H2O (0.291g, 1mmol), H2PA (0.388g, 1mmol), bpp (0.198g, 1mmol) and KOH (0.112g, 2mmol) in DMF?H2O?MeOH (1:2:2) (10mL) was heated for 72h at 110°C in a Teflon-lined stainless steel vessel (23mL). The reaction system was then cooled to room temperature and green block crystals of 4 were collected, washed with water and dried in air (yield 36percent). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
58% | at 140℃; for 72h;High pressure; | A mixture of 5-Br-H2ip (24.3mg, 0.1 mmol), bpp (0.1 mmol,18.4 mg), CdCl2 (18.3 mg, 0.1 mmol) and H2O (10 mL) was placed in a Teflon-lined stainless steel vessel, heated to 140 °C for 3 days, and then cooled to room temperature over 24 h. Colorless block crystals of 2 were obtained. Yield: 58percent basedon Cd. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
82% | In ethanol; water; at 20℃; | The complex was synthesized by addition of 4,4'-trimethylenedipyridine (6.2 mg, 0.031 mmol) and <strong>[27148-03-4]thiosaccharine</strong> (12.7 mg, 0.0638 mmol), respectively, to a solution of Zn(NO3)26H2O (10.2mg, 0.0342 mmol) in ethanol:water (4 ml), and kept under mechanical stirring at room temperature. The resulting yellow solid was filtered off and washed with cold water. By slow evaporation of the mother solution single crystals appeared. They were washed with water and analysed using X-ray diffraction. Yield: 82%. Molar conductivity (mS M1) = 28.3. Analytical percent composition calculated for C27H22N4O4S4Zn: C = 49.127%; H = 3.359%;N = 8.487%. Found: C = 48.811%; H = 2.981%; N = 8.378%. Soluble in DMSO and DMF. Slightly soluble in water, ethanol, methanol, chloroform. Insoluble in acetone and methane dichloride. UV-Visible [DMSO, kmax nm]: 347.1H NMR (300 MHz, DMSO) d 8.46 (dd, 4H), 7.92 (m, 2H), 7.58-7.72 (m, 6H), 7.28 (dd, 4H), 2.64 (t, 4H), 1.93 (m, 2H). 13C NMR (75 MHz, DMSO) d 191.71 (C1), 151.07 (C10), 149.31 (C8), 137.98(C7), 136.56 (C2), 132.05 (C4), 130.82 (C5), 125.07 (C3), 124.04(C9), 119.01 (C6), 33.80 (C11), 30.12 (C12). |