Bis(phenylphosphonic) anhydride
نویسندگان
چکیده
منابع مشابه
Bis(phenylphosphonic) anhydride
The asymmetric unit of the title compound, C(12)H(12)O(5)P(2), contains four independent mol-ecules, generating two dimers via pairs of inter-molecular O-H⋯O hydrogen bonds, forming R(2) (2)(8) rings. The two aryl rings of each mol-ecule form dihedral angles of 108.6 (1), 103.2 (1), 12.5 (2) and 8.1 (2)° in the four mol-ecules.
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The complete mol-ecule of the title compound, C(26)H(20)N(2)O(3), is generated by crystallographic twofold symmetry, with the central O atom lying on the rotation axis. The conformation is stabilized by an intra-molecular N-H⋯O hydrogen bond. The dihedral angle between the inner and outer aromatic ring planes is 61.12 (5)°.
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The reversible reaction of exo-cis-3,6-endo-epoxy-4,5-cis-epoxyhexahydrophthalic anhydride (EEHPA) with free protein amino groups is described. The free protein amino groups of lysozyme can be completely blocked through the reaction of the anhydride EEHPA. The chemically less reactive epoxy groups in EEHPA-modified lysozyme remain intact during modification of the protein and can be used for ma...
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THE TITLE COMPOUND [SYSTEMATIC NAME: 2-(4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octa-hydro-naphthalen-2-yl)acrylic acid anhydride], C(30)H(42)O(3), is a new isocostic anhydride which was synthesized from the aerial part of Inula Viscosa- (L) Aiton [or Dittrichia Viscosa- (L) Greuter]. The mol-ecule adopts an essentially linear shape with two terminal fused-rings bridged by the anhydride group. The exte...
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The difructose anhydrides include four welldefined crystalline sugars. Diheterolevulosan was first prepared by Pictet and Chavan [1]l by the action of concentrated hydrochloric acid on fructose at 0° C. This sugar is a difructopyranose in which carbon atoms 1 and 2 of each fructose residue are joined to form a dioxane ring. The other members [2,3] of this group arc designated difructose anhydri...
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ژورنال
عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online
سال: 2009
ISSN: 1600-5368
DOI: 10.1107/s1600536809038525