1,1′-Binaphthyl-2,2′-dicarboxylic acid–urea (1/1)

نویسندگان

  • Lidiya Izotova
  • Jamshid Ashurov
  • Samat Talipov
  • Bakhtiyar Ibragimov
  • Edwin Weber
چکیده

In the title co-crystal, C(22)H(14)O(4)·CH(4)N(2)O, the 1,1'-binaphthyl-2,2'-dicarboxylic acid (BNDA) and urea mol-ecules are connected via a system of hydrogen bonds into a chiral two-dimensional polymeric structure parallel to the (001) plane. As the crystal is centrosymmetric, it consists of alternately stacked BNDA-urea layers of opposite chirality. The urea H atoms trans to the C=O group are bonded in a chelating mode [R(1) (2)(6)] to the carbonyl O atom from one of the carboxylic acid groups which, in turn, acts as the donor of an O-H⋯O hydrogen bond to another urea mol-ecule. The [010] chains thus formed are further connected via an R(2) (2)(8) hydrogen-bond motif formed between urea and the second carboxylic acid group of BNDA.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A coincident spontaneous resolution system for racemic 1,1'-binaphthyl-2,2'-dicarboxylic acid and 1,2-diphenylethylenediamine induced by water.

Spontaneously resolvable conglomerate crystals are obtained by combining racemic (rac)-1,1'-binaphthyl-2,2'-dicarboxylic acid and rac-1,2-diphenylethylenediamine, and this spontaneous resolution system is induced by water which is present in the crystallization solvent.

متن کامل

Enthalpy/entropy contributions to conformational KIEs: theoretical predictions and comparison with experiment.

Previous theoretical studies of Mislow's doubly-bridged biphenyl ketone 1 and dihydrodimethylphenanthrene 2 have determined significant entropic contributions to their normal (1) and inverse (2) conformational kinetic isotope effects (CKIEs). To broaden our investigation, we have used density functional methods to characterize the potential energy surfaces and vibrational frequencies for ground...

متن کامل

Synthesis and characterization of group 4 metal amides with new C2-symmetric binaphthyldiamine-based ligands and their use as catalysts for asymmetric hydroamination/cyclization.

A new series of titanium(IV) and zirconium(IV) amides have been prepared from the reaction between M(NMe(2))(4) (M = Ti, Zr) and chiral ligands, (R)-2,2'-bis(p-toluenesulfonylamino)-1,1'-binaphthyl (1H(2)), (R)-2,2'-bis(diphenylphosphinoylamino)-1,1'-binaphthyl (2H(2)), (R)-2,2'-bis(mesitoylamino)-1,1'-binaphthyl (3H(2)), (R)-5,5',6,6',7,7',8,8'-octahydro-2,2'-bis(pyrrol-2-ylmethyleneamino)-1,1...

متن کامل

catena-Poly[[trimethyl­tin(IV)]-μ-(1,1′-binaphthyl-2,2′-diyl phospho­nato)]

In the title polymeric coordination compound, [Sn(CH(3))(3)(C(20)H(12)O(4)P)](n), the Sn atom exhibits a distorted trigonal-bipyramidal coordination geometry with the phosphate O atoms of the 1,1'-binaphthyl-2,2'-diyl phospho-nate ligands in axial positions and equatorial sites occupied by the three methyl groups. Adjacent Sn atoms are bridged by coordination to the two O atoms of each 1,1'-bin...

متن کامل

Economy of Catalyst Synthesis-Convenient Access to Libraries of Di- and Tetranaphtho Azepinium Compounds.

Efficient optimization procedures in chiral catalysis are usually linked to a straightforward strategy to access groups of structurally similar catalysts required for fine-tuning. The ease of building up such ligand libraries can be increased when the structure-modifying step (introduction of a substituent) is done at a later stage of the synthesis. This is demonstrated for the extended family ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 64  شماره 

صفحات  -

تاریخ انتشار 2008