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ÑôÃ÷sir: ½ð±Ò+20, ²©Ñ§EPI+1, ¡ï¡ï¡ïºÜÓаïÖú, лÁË 2015-09-13 10:47:32
[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
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ÑôÃ÷sir: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ¶àл 2015-09-13 10:47:46
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
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3Â¥2015-09-12 17:44:59
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