Coordination Chemistry of ADPO

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
   Google Scholar
• Stewart , C. A. and Arduengo , A. J. III . 1986 . Inorg. Chem. , 25 : 3847
   Web of Science ®Google Scholar
• Arduengo , A. J. III , Lattman , M. , Calabrese , J. C. and Fagan , P. J. 1990 . Heteroat. Chem. , 1 : 407
   Google Scholar
• Arduengo , A. J. III , Lattman , M. , Dias , H. V. R. , Calabrese , J. C. and Kline , M. 1991 . J. Am. Chem. Soc. , 113 : 1799
   Web of Science ®Google Scholar
• 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
   Web of Science ®Google Scholar
• 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
   Web of Science ®Google Scholar
• Arduengo , A. J. III , Dias , H. V. R. and Calabrese , J. C. 1991 . J. Am. Chem. Soc. , 113 : 7071
   Web of Science ®Google Scholar
• Arduengo , A. J. III , Dias , H. V. R. and Calabrese , J. C. 1991 . Inorg. Chem. , 30 : 4880
   Web of Science ®Google Scholar
• Arduengo , A. J. III , Stewart , C. A. and Davidson , F. 1986 . J. Am. Chem. Soc. , 108 : 322
   Web of Science ®Google Scholar
• Arduengo , A. J. III , Lattman , M. , Dixon , D. A. and Calabrese , J. C. 1991 . Heteroat. Chem. , 2 : 395
   Google Scholar
• 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 .
   Google Scholar
• Muetterties , E. L. and Alegranti , C. W. 1972 . J. Am. Chem. Soc. , 94 : 6386
   Web of Science ®Google Scholar
• Arif , A. M. , Cowley , A. H. , Norman , N. C. , Orpen , A. G. and Pakulski , M. 1988 . Organometallics , 7 : 309
   Web of Science ®Google Scholar
• 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
   Web of Science ®Google Scholar
• Huttner , G. and Evertz , K. 1986 . Acc. Chem. Res. , 19 : 406
   Web of Science ®Google Scholar
• Lang , H. , Hutmer , G. and Jibril , I. 1986 . Z. Naturforsch. , 41b : 473
   Google Scholar
• Hinke , A.-M. , Hinke , A. , Kuchen , W. and Hsnle , W. 1986 . Z. Naturforsch. , 41b : 629
   Google Scholar
• Lang , H. , Orama , O. and Huttner , G. 1985 . J. Organomet. Chem. , 291 : 293
   Web of Science ®Google Scholar
• Weber , U. , Zsolnai , L. and Hutmer , G. 1984 . J. Organomet. Chem. , 260 : 281
   Web of Science ®Google Scholar
• Huttner , G. , Borm , J. and Zsolnai , L. 1984 . J. Organomet. Chem. , 263 : C33
   Web of Science ®Google Scholar
• Herrmann , W. , Koumbouris , B. , Zahn , T. and Ziegler , M. L. 1984 . Angew. Chem., Int. Ed. Engl. , 23 : 812
   Web of Science ®Google Scholar
• Jones , R. A. and Whittlesey , B. R. 1984 . Organometallics , 3 : 469
   Web of Science ®Google Scholar
• Flynn , K. M. , Murray , B. D. , Olmstead , M. M. and Power , P. P. 1983 . J. Am. Chem. Soc. , 105 : 7060
   Google Scholar
• Sigwarth , B. , Zsolnai , L. , Scheidsteger , O. and Huttner , G. 1982 . J. Organomet. Chem. , 235 : 43
   Web of Science ®Google Scholar
• von Seyerl , J. , Sigwarth , B. , Schmid , H. , Mohr , G. , Frank , A. , Marsili , M. and Huttner , G. 1981 . Chem. Ber. , 114 : 1392
   Google Scholar
• von Seyerl , J. , Moering , U. , Wagner , A. , Frank , A. and Huttner , G. 1978 . Angew. Chem., Int. Ed. Engl. , 17 : 844
   Web of Science ®Google Scholar
• 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)
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• 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
   Google Scholar
• Bonningue , C. , Houalla , D. , Sanchez , M. and Wolf , R. 1981 . J. Chem. Soc., Perkin Trans. II , 1 : 9
   Google Scholar
• Bonningue , C. , Houalla , D. and Wolf , R. 1983 . J. Chem. Soc., Perkin Trans., II , 77 : 3
   Google Scholar
• Perrin , D. D. , Armarego , W. L. F. and Perrin , D. R. 1985 . Purification of Laboratory Chemicals , New York : Pergamon .
   Google Scholar