Phosphide delivery to a cyclotrisilene

Angewandte Chemie - International Edition

Volumn 54, Issue 2, 2015, Pages 683-686

  Robinson, Thomas P ^a   Cowley, Michael J ^b,c   Scheschkewitz, David ^b   Goicoechea, Jose M ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b SAARLAND UNIVERSITY   (Germany)

^c UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

2 phosphaethynolate; Main group chemistry; Multiple bonds; Silenes; Silicon

Indexed keywords

CHEMICAL BONDS; SCAFFOLDS;

2-PHOSPHAETHYNOLATE; CYCLOBUTENE; DECARBONYLATIONS; DOUBLE BONDS; MAIN GROUP CHEMISTRY; MULTIPLE BONDS; SILENES;

SILICON;

EID: 84922795705     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201409908     Document Type: Article

References (54)

1. a) R. J. Hamers, U. K. Köhler, J. E. Demuth, Ultramicroscopy 1989, 31, 10-19;
2. b) M. T. Swihart, S. L. Girshick, J. Phys. Chem. B 1999, 103, 64-76;
3. c) M. T. Swihart, S. L. Girshick, Chem. Phys. Lett. 1999, 307, 527-532;
4. d) N. Ning, H. Vach, J. Phys. Chem. A 2010, 114, 3297-3305;
5. e) W. O. Filtvedt, A. Holt, P. A. Ramachandran, M. C. Melaaen, Sol. Energy Mater. Sol. Cells 2012, 107, 188-200.
6. T. Iwamoto, C. Kabuto, M. Kira, J. Am. Chem. Soc. 1999, 121, 886-887.
7. M. Ichinohe, T. Matsuno, A. Sekiguchi, Angew. Chem. Int. Ed. 1999, 38, 2194-2196;
8. Angew. Chem. 1999, 111, 2331-2333.
9. a) K. Leszczyńska, K. Abersfelder, A. Mix, B. Neumann, H.-G. Stammler, M. J. Cowley, P. Jutzi, D. Scheschkewitz, Angew. Chem. Int. Ed. 2012, 51, 6785-6788;
10. Angew. Chem. 2012, 124, 6891-6895;
11. b) M. J. Cowley, V. Huch, H. S. Rzepa, D. Scheschkewitz, Nat. Chem. 2013, 5, 876-879.
12. S. M. Sze, K. K. Ng, Physics of Semiconductor Devices, 3rd ed., Wiley, Hoboken, 2007.
13. a) G. Fritz, P. Scheer, Chem. Rev. 2000, 100, 3341-3401;
14. b) C. von Hänisch, Z. Anorg. Allg. Chem. 2008, 634, 23-29.
15. a) C. N. Smit, F. Bickelhaupt, Organometallics 1987, 6, 1156;
16. b) M. Driess, Angew. Chem. Int. Ed. Engl. 1991, 30, 1022-1024;
17. Angew. Chem. 1991, 103, 979-981;
18. c) M. Driess, S. Rell, H. Pritzkow, R. Janoschek, Angew. Chem. Int. Ed. Engl. 1997, 36, 1326-1329;
19. Angew. Chem. 1997, 109, 1384-1387;
20. d) M. Driess, S. Block, M. Brym, M. T. Gamer, Angew. Chem. Int. Ed. 2006, 45, 2293-2296;
21. Angew. Chem. 2006, 118, 2351-2354;
22. e) V. Y. Lee, M. Kawai, A. Sekiguchi, H. Ranaivonjatovo, J. Escudié, Organometallics 2009, 28, 4262-4265;
23. f) K. Hansen, T. Szilvási, B. Blom, E. Irran, M. Driess, Chem. Eur. J. 2014, 20, 1947-1956;
24. g) P. Willmes, M. J. Cowley, M. Hartmann, M. Zimmer, V. Huch, D. Scheschkewitz, Angew. Chem. Int. Ed. 2014, 53, 2216-2220;
25. Angew. Chem. 2014, 126, 2248-2252.
26. M. Hartmann, A. Haji-Abdi, K. Abersfelder, P. R. Haycock, A. J. P. White, D. Scheschkewitz, Dalton Trans. 2010, 39, 9288-9295.
27. Y. Ohmori, M. Ichinohe, A. Sekiguchi, M. J. Cowley, V. Huch, D. Scheschkewitz, Organometallics 2013, 32, 1591-1594.
28. a) M. J. Cowley, Y. Ohmori, V. Huch, M. Ichinohe, A. Sekiguchi, D. Scheschkewitz, Angew. Chem. Int. Ed. 2013, 52, 13247-13250;
29. Angew. Chem. 2013, 125, 13489-13492;
30. b) M. J. Cowley, V. Huch, D. Scheschkewitz, Chem. Eur. J. 2014, 20, 9221-9224.
31. A. M. Tondreau, Z. Benko{combining double acute accent}, J. R. Harmer, H. Grützmacher, Chem. Sci. 2014, 5, 1545-1554.
32. G. Becker, W. Schwarz, N. Seidler, M. Westerhausen, Z. Anorg. Allg. Chem. 1992, 612, 72-82.
33. F. F. Puschmann, D. Stein, D. Heift, C. Hendriksen, Z. A. Gal, H.-F. Grützmacher, H. Grützmacher, Angew. Chem. Int. Ed. 2011, 50, 8420-8423;
34. Angew. Chem. 2011, 123, 8570-8574.
35. D. Heift, Z. Benko{combining double acute accent}, H. Grützmacher, Dalton Trans. 2014, 43, 831-840.
36. A. R. Jupp, J. M. Goicoechea, Angew. Chem. Int. Ed. 2013, 52, 10064-10067;
37. Angew. Chem. 2013, 125, 10248-10251.
38. X. Chen, S. Alidori, F. F. Puschmann, G. Santiso-Quinones, Z. Benko{combining double acute accent}, Z. Li, G. Becker, H.-F. Grützmacher, H. Grützmacher, Angew. Chem. Int. Ed. 2014, 53, 1641-1645;
39. Angew. Chem. 2014, 126, 1667-1671.
40. D. Heift, Z. Benko{combining double acute accent}, H. Grützmacher, Angew. Chem. Int. Ed. 2014, 53, 6757-6761;
41. Angew. Chem. 2014, 126, 6875-6879.
42. CCDC via www.ccdc.cam.ac.uk/Community/Requestastructure/Pages/DataRequest.aspx.
43. M. D. Levin, P. Kaszynski, J. Michl, Chem. Rev. 2000, 100, 169-234.
44. T. Iwamoto, D. Tsushima, E. Kwon, S. Ishida, H. Isobe, Angew. Chem. Int. Ed. 2012, 51, 2340-2344;
45. Angew. Chem. 2012, 124, 2390-2394.
46. A. Rammo, I. Bejan, A. Meltzer, K. Radacki, H. Braunschweig, D. Scheschkewitz, Aust. J. Chem. 2013, 66, 1311-1314.
47. a) B. Cordero, V. Gómez, A. E. Platero-Prats, M. Revés, J. Echeverría, E. Cremades, F. Barragán, S. Alvarez, Dalton Trans. 2008, 2832-2838;
48. b) P. Pyykkö, M. Atsumi, Chem. Eur. J. 2009, 15, 186-197.
49. Calculations were carried out with the Gaussian09 program package: Gaussian09 (Revision D.01), M. J. Frisch, et al., Gaussian, Inc., Wallingford CT, 2013.
50. a) M. Ichinohe, Y. Arai, A. Sekiguchi, N. Takagi, S. Nagase, Organometallics 2001, 20, 4141-4143;
51. b) K. Abersfelder, D. Scheschkewitz, J. Am. Chem. Soc. 2008, 130, 4114-4121.
52. D. Auer, C. Strohmann, A. V. Arbuznikov, M. Kaupp, Organometallics 2003, 22, 2442-2449.
53. T. Matsuno, M. Ichinohe, A. Sekiguchi, Angew. Chem. Int. Ed. 2002, 41, 1575-1577;
54. Angew. Chem. 2002, 114, 1645-1647.