Assignment of 31P Chemical Shifts to Isomers of 2,3-Dialkoxy-A3-diazadiphosphetidines — Crystal and Molecular Structure of rrflMs-[PhNP(OCH2CF3)]2

نویسندگان

  • S. S. Kumaravel
  • S. S. Krishnamurthy
  • T. S. Cameron
چکیده

Geometrical isomers of /.3-diazadiphosphetidines show large differences in their 31P chemical shifts. Trifluoroethoxylation of rä-(PhNPC l) 2 gives only the 'low-field' isomer initially, for which the crystal structure is determined. The compound crystallises in the triclinic space group P 1 with a = 9 .624(4 ).6 = 10 .107(4),c = 11.140(7) Ä ;a = 105.65(4),ß = 110.59(4),y = 93 .82(3)°;and Z = 2. The structure was solved by direct methods and refined to R = 0.045. The alkoxy groups are trans to each other. On standing in solution. rra/J5 -[PhNP(OCH 2 CF3 ) ] 2 transforms slowly and almost com pletely into its cis analogue with a high field 31P chemical shift.

برای دانلود رایگان 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

Quantum Chemical Investigations on C14C10-Branched-Chain Glucoside Isomers Towards Understanding Self-Assembly

Density Functional Theory (DFT) calculations have been carried out using a Polarizable Continuum Model (PCM) in an attempt to investigate the electro-molecular properties of branched-chain glucoside (C14C10-D-glucoside) isomers. The results showed that αconfiguration of pyranoside form is thermodynamically the most stable, while the solution should contain much more β...

متن کامل

Theoretical investigations on molecular structure, NBO, HOMO-LUMO and MEP analysis of two crystal structures of N-(2-benzoyl-phenyl) oxalyl: A DFT study

The N-(2-benzoyl-phenyl) oxalyl derivatives are important models for studying of three-centered intramolecular hydrogen bonding in organic molecules. The quantum theoretical calculations for two crystal structures of N-(2-benzoyl-phenyl) oxalyl (compounds I and II) were performed by Density Functional Theory (B3LYP method and 6-311+G* basis set). From the optimized structures, geometric paramet...

متن کامل

Synthesis and crystal structures of 2,3,12,13-tetraalkoxy-21,23-dithiaporphyrins and 2,3-dialkoxy-21-monothiaporphyrins

The tetraalkoxy and dialkoxy substituted 21,23-dithiaporphyrins and 21-monothiaporphyrins, respectively, having methoxy, butoxy, octyloxy and dodecyloxy substituents at b-thiophene carbons were synthesized and characterized. The X-ray structure was solved for tetrabutoxy substituted 21,23-dithiaporphyrin and it exhibited a more planar structure compared with unsubstituted S2TPP, whereas the dim...

متن کامل

The Biophysical Probes 2-fluorohistidine and 4-fluorohistidine: Spectroscopic Signatures and Molecular Properties

Fluorinated amino acids serve as valuable biological probes, by reporting on local protein structure and dynamics through 19F NMR chemical shifts. 2-fluorohistidine and 4-fluorohistidine, studied here with DFT methods, have even more capabilities for biophysical studies, as their altered pKa values, relative to histidine, allow for studies of the role of proton transfer and tautomeric state in ...

متن کامل

Effect of Alkyl Substituents on the Hydrogen Bonding and Molecular Structure of Benzophenylhydroxamic Acids Crystal structure of UO2 Complex of p-Isopropylbenzophenylhydroxamic Acid

The effect of alkyl substituents on the C-phenyl and/or the N-Phenyl ring of benzophenylhydroxamic acid on their molecular structure and hydrogen bonding has been investigated. The predominant configuration in CHCl3 is determined by steric and electronic effects. Substituents on the C-phenyl ring favor the cis configuration, while substituents in the N-phenyl ring favor a trans c...

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

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2012