3
82
GUSAROVA et al.
С Н ClРSe. Calculated, %: 54.03; H 5.10; Cl 9.97; P
2006, vol. 348, no. 18, p. 2609. DOI: 10.1002/
adsc.200606171.
1
6
18
8
.71; Se 22.20.
3
4
. Das, P., Bora, U., Tairai, A., and Sharma, C., Tetra-
hedron Lett., 2010, vol. 51, no. 11, p. 1479. DOI:
Bis[2-(2-phenyl)propyl]selenophosphorylchloride
–
1
(
5
VI). Yield 90%, viscous liquid. IR spectrum, ν, cm :
1
0.1016/j.tetlet.2010. 01.032.
1
10 (P=Se). H NMR spectrum (CDCl ), δ, ppm: 1.27
3
. Arbuzova, S.N., Volkov, P.A., Ivanova, N.I., Gusaro-
va, N.K., Larina, L.I., Kazheva, O.N., Alexandrov, G.G.,
Dyachenko, O.A., and Trofimov, B.A., J. Organomet.
Chem., 2011, vol. 696, no. 10, p. 2053. DOI: 10.1016/
j.jorganchem.2010.10.062.
3
3
d and 1.33 (3H, MeCH, J 7.0, J 6.6 Hz), 1.35 d
and 1.39 d (3H, MeCH, J 6.7, J 7.0 Hz); 2.24–
HP
HP
3
3
HP
HP
2
3
.31 m, 2.38–2.47 m, and 2.51–2.57 m (4H, CH P),
2
1
3
.31–3.55 m (2H, PhCH), 7.07–7.27 m (10H, Ph). C
3
NMR spectrum, δ , ppm: 22.88 d (MeCH, JCP
5. Ishikawa, H., Kido, T., Umeda, T., and Ohyama H.,
Biosci. Biotech. Biochem., 1992, vol. 56, no. 11, p. 1882.
DOI: 10.1271/bbb.56.1880.
6. Dehghanpour, S., Rasmi, Y, and Bagheri, M., Mol.
Divers., 2007, vol. 11, no. 1, p. 47. DOI: 10.1007/
s11030-007-9056-6.
С
3
1
(
3
1.2 Hz), 23.30 d (MeCH, J 12.5 Hz), 23.85 d
CP
3
3
MeCH, J 12.1 Hz), 23.99 d (MeCH, J 11.2 Hz),
CP CP
2
2
5.85 d (PhCH, J 4.3 Hz), 36.11 (PhCH, J
CP
CP
2
1
.7 Hz), 36.32 d (PhCH, J 3.5 Hz), 35.41 d (PhCH,
JCP 2.4 Hz), 49.15d (CH P, J 41.4 Hz), 49.57 d
CH P, J 41.4 Hz), 49.74 d (CH P, J 41.8 Hz),
CP
2
1
2
CP
1
1
7
. Chauhan, H.P.S., Singh, U.P., Shaik, N.M., and
Bhatiya, S., Main Group Metal Chem., 2007, vol. 30,
no. 5, p. 279. DOI: 10.1515/MGMC.2007.30.5.279.
(
2 CP 2 PC
1
5
1
0.06 d (CH P, J 43.1 Hz), 126.71–127.24 m and
2 CP
o
m
p
ipso
28.58–128.73 m (C , C , C ), 145.50–145.80 m (C ).
3
1
8. Bochmann, M., Bwembya, G.C., Hursthouse, M.B., and
Coles, S.J.J., J. Chem. Soc. Dalton Trans., 1995,
p. 2813. DOI: 10.1039/DT9950002813.
P NMR spectrum, δ , ppm: 88.37 (+ doublet of
Р
1
satellites, JPSe 822.2 Hz), 89.72 (+ doublet of
1
satellites, 1 JPSe 825.9 Hz), 91.07 (+ doublet of
77
9. Song, X. and Bochmann, M., J. Chem. Soc. Dalton
Trans., 1997, p. 2689. DOI: 10.1039/A702460F.
satellites, J
ppm: –78.9 d ( J
825.9 Hz). Se NMR spectrum, δ ,
PSe
Se
1
1
822.2 Hz), –100.2 d ( J
25.9 Hz), –116.3 d ( JPSe 825.9 Hz). Found, %: C
6.71; H 5.70; Cl 9.27; P 8.02; Se 20.49. С Н ClРSe.
PSe
PSe
1
10. Ruberu, T.P.A., Albright, H.R., Callis, B., Ward, B.,
Cisneros, J., Fan, H.-J., and Vela, J., ACS Nano, 2012,
vol. 6, no. 6, p. 5348. DOI: 10.1021/nn301182h.
8
5
1
8
22
Calculated, %: C 56.34; H 5.78; Cl 9.24; P 8.07; Se
0.58.
1
1. Hodgson, L.M., Platel, R.H., White, A.J.P., and
Williams, C.K., Macromolecules, 2008, vol. 41, no. 22,
p. 8603. DOI: 10.1021/ma8016663.
2
ACKNOWLEDGMENTS
This work financially supported from Council on
grants of President of Russian Federation for state
support of leading scientific schools (project NSH-
1
2. Hoque, M.E.U. and Lee, H.W., Bull. Korean Chem.
Soc., 2011, vol. 32, no. 7, p. 2306. DOI: dx.doi.org/
1
0.5012/bkcs.2011. 32.7.2306.
1
1
1
1
3. Kuchen, W. and Knop, B., Angew. Chem., 1964,
vol. 76, no. 11, p. 496. DOI: 10.1002/ange.19640761112.
1
56.2014.3).
4. Kimura, T. and Murai, T., Chem. Lett., 2004, vol. 33,
no. 7, p. 878. DOI: 10.1246/cl.2004.878.
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