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- ²©Ñ§EPI: 11
- Ó¦Öú: 95 (³õÖÐÉú)
- ½ð±Ò: 4173
- É¢½ð: 81
- ºì»¨: 21
- Ìû×Ó: 679
- ÔÚÏß: 187.7Сʱ
- ³æºÅ: 3366683
- ×¢²á: 2014-08-14
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
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ÑôÃ÷sir: ½ð±Ò+20, ²©Ñ§EPI+1, ¡ï¡ï¡ïºÜÓаïÖú, лÁË 2015-09-13 10:47:32
ÑôÃ÷sir: ½ð±Ò+20, ²©Ñ§EPI+1, ¡ï¡ï¡ïºÜÓаïÖú, лÁË 2015-09-13 10:47:32
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[Pd(CH3CN)2Cl2]. The procedure is adapted from that already described for the corresponding benzonitrile complexes.57 Palladium chloride was suspended in acetonitrile (120 ml CH3CN per gram of PdCl2) and refluxed for 2 h allowing PdCl2 to essentially dissolve completely. The hot solution was filtered through filtering paper with the aid of a cannula to remove very small amounts of undissolved impurities. The solution was then cooled at 0 ¡ãC to promote [Pd(CH3CN)2Cl2] precipitation. The yellow solid was recovered by filtration with a Buchner. The remaining solution was then evaporated in vacuo to afford additional complex (quantitative yield). Calcd for C4H6N2Cl2Pd: C, 18.52; H, 2.33; N, 10.80%. Found: C, 18.78, H, 2.26; N, 10.72%. ¦ÄH (CDCl3, RT, 300 MHz): 2,40 (s, CH3). The spectrum also shows a signal at 2.03 ppm indicating free acetonitrile. Aweak signal at 2.39 ppm is also observable. IR (nujol): 2335, 2304 cm−1 (in accord with the literature58) IR (C2H4Cl2): 2337, 2306 cm−1. Dalton Trans., 2012,41, 3648-3658 ÕâÊÇ×öÂÈ»¯îÙÒÒëæÅäºÏÎïµÄ£¬Ëû¾ÍÊÇÏȰÑPdCl2·ÅÔÚÒÒëæÀï¼ÓÈÈ»ØÁ÷£¬ÈÃÆäÈܽ⣬Ȼºó½µÎÂÎö¾§¡£ËùÒÔÇ°ÃæÈܽâµÄ²¿·Ö¿ÉÒԲο¼ |

2Â¥2015-09-12 17:43:13
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- ²©Ñ§EPI: 11
- Ó¦Öú: 95 (³õÖÐÉú)
- ½ð±Ò: 4173
- É¢½ð: 81
- ºì»¨: 21
- Ìû×Ó: 679
- ÔÚÏß: 187.7Сʱ
- ³æºÅ: 3366683
- ×¢²á: 2014-08-14
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
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ÑôÃ÷sir: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ¶àл 2015-09-13 10:47:46
ÑôÃ÷sir: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ¶àл 2015-09-13 10:47:46
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Bis(acetonitrile)dichloropalladium(II), Pd(MeCN)2Cl2, was prepared from PdCl2 as described: PdCl2 (2.0 g, 11.3 mmol) was suspended in dry MeCN (450 mL). The reaction mixture was heated to reflux for 3 hours under argon atmosphere. After cooling down to room temperature (23¡ãC) the solvent was removed under reduced pressure. The remaining solid was dried under high vacuum and the title compound was received in quantitative yield (2.9 g) as an orange-yellow solid. The dried product can be used without further purification and was stored under argon in the dark¡£ Org. Lett. 2015, 17, 2478−2481 ÀàËÆµÄ |

3Â¥2015-09-12 17:44:59














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