References
- The ADPnO acronym has been previously described and is used for simplicity in place of the name of the ring system it represents: 5-aza-2,8-dioxa-1-pnictabicyclo[3.3.0]octa-2,4,6-triene. See reference 5, footnote id for details
- Stewart , C. A. and Arduengo , A. J. III . 1986 . Inorg. Chem. , 25 : 3847
- Arduengo , A. J. III , Lattman , M. , Calabrese , J. C. and Fagan , P. J. 1990 . Heteroat. Chem. , 1 : 407
- Arduengo , A. J. III , Lattman , M. , Dias , H. V. R. , Calabrese , J. C. and Kline , M. 1991 . J. Am. Chem. Soc. , 113 : 1799
- Arduengo , A. J. III , Stewart , C. A. , Davidson , F. , Dixon , D. A. , Becker , J. Y. , Culley , S. A. and Mizen , M. B. 1987 . J. Am. Chem. Soc. , 109 : 627
- Perkins , C. W. , Martin , J. C. , Arduengo , A. J. III , Lau , W. , Algeria , A. and Kochi , J. K. 1980 . J. Am. Chem. Soc. , 102 : 7753 The N-X-L, nomenclature system has been previously described, N, valence electrons about a central atom X, with L, ligands
- Arduengo , A. J. III , Dias , H. V. R. and Calabrese , J. C. 1991 . J. Am. Chem. Soc. , 113 : 7071
- Arduengo , A. J. III , Dias , H. V. R. and Calabrese , J. C. 1991 . Inorg. Chem. , 30 : 4880
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- Arduengo , A. J. III , Lattman , M. , Dixon , D. A. and Calabrese , J. C. 1991 . Heteroat. Chem. , 2 : 395
- Arduengo , A. J. III and Dixon , D. A. 1990 . “ Electron Rich Bonding at Low Coordination Main Group Element Centers ” . In Heteroatom Chemistry: ICHAC-2; , Edited by: Block , E. 47 New York : VCH .
- Muetterties , E. L. and Alegranti , C. W. 1972 . J. Am. Chem. Soc. , 94 : 6386
- Arif , A. M. , Cowley , A. H. , Norman , N. C. , Orpen , A. G. and Pakulski , M. 1988 . Organometallics , 7 : 309
- Bartlett , R. A. , Dias , H. V. R. , Flynn , K. M. , Hope , H. , Murray , B. D. , Olmstead , M. M. and Power , P. P. 1987 . J. Am. Chem. Soc. , 109 : 5693
- Huttner , G. and Evertz , K. 1986 . Acc. Chem. Res. , 19 : 406
- Lang , H. , Hutmer , G. and Jibril , I. 1986 . Z. Naturforsch. , 41b : 473
- Hinke , A.-M. , Hinke , A. , Kuchen , W. and Hsnle , W. 1986 . Z. Naturforsch. , 41b : 629
- Lang , H. , Orama , O. and Huttner , G. 1985 . J. Organomet. Chem. , 291 : 293
- Weber , U. , Zsolnai , L. and Hutmer , G. 1984 . J. Organomet. Chem. , 260 : 281
- Huttner , G. , Borm , J. and Zsolnai , L. 1984 . J. Organomet. Chem. , 263 : C33
- Herrmann , W. , Koumbouris , B. , Zahn , T. and Ziegler , M. L. 1984 . Angew. Chem., Int. Ed. Engl. , 23 : 812
- Jones , R. A. and Whittlesey , B. R. 1984 . Organometallics , 3 : 469
- Flynn , K. M. , Murray , B. D. , Olmstead , M. M. and Power , P. P. 1983 . J. Am. Chem. Soc. , 105 : 7060
- Sigwarth , B. , Zsolnai , L. , Scheidsteger , O. and Huttner , G. 1982 . J. Organomet. Chem. , 235 : 43
- von Seyerl , J. , Sigwarth , B. , Schmid , H. , Mohr , G. , Frank , A. , Marsili , M. and Huttner , G. 1981 . Chem. Ber. , 114 : 1392
- von Seyerl , J. , Moering , U. , Wagner , A. , Frank , A. and Huttner , G. 1978 . Angew. Chem., Int. Ed. Engl. , 17 : 844
- The symbol {ADPO}2 is used to represent the dimerized ADPO unit in which two 5-membered rings have joined at their P-O bonds to form a 10-membered ring (eq 3)
- This drawing was made with the KANVAS, computer graphics program. This program is based on the program SCHAKAL, of E. Keller (Kristallographisches Institute der Universitat Freiburg, Germany), which was modified by A. J. Arduengo, III (E. I. du Pont de Nemours & Co., Wilmington, DE) to produce the back and shadowed planes. The planes bear a 50-pm grid and the lighting source is at infinity so that shadow size is meaningful
- Bonningue , C. , Houalla , D. , Sanchez , M. and Wolf , R. 1981 . J. Chem. Soc., Perkin Trans. II , 1 : 9
- Bonningue , C. , Houalla , D. and Wolf , R. 1983 . J. Chem. Soc., Perkin Trans., II , 77 : 3
- Perrin , D. D. , Armarego , W. L. F. and Perrin , D. R. 1985 . Purification of Laboratory Chemicals , New York : Pergamon .