Chuanjiang Hu

Summary

Affiliation: Suzhou University
Country: China

Publications

  1. pmc Effects of imidazole deprotonation on vibrational spectra of high-spin iron(II) porphyrinates
    Chuanjiang Hu
    Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P R China
    Inorg Chem 52:3170-7. 2013
  2. doi request reprint Chiral recognition of amino acid esters by a novel oxalic amide-linked bisporphyrin
    Jiaxun Jiang
    Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China
    Dalton Trans 42:7651-9. 2013
  3. pmc Nuclear resonance vibrational spectra of five-coordinate imidazole-ligated iron(II) porphyrinates
    Chuanjiang Hu
    Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China
    Inorg Chem 51:1359-70. 2012
  4. pmc Electronic configuration of five-coordinate high-spin pyrazole-ligated iron(II) porphyrinates
    Chuanjiang Hu
    Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China
    Inorg Chem 49:10984-91. 2010
  5. doi request reprint Facile one-pot synthesis of unprecedented β,β'-linked porphyrin-chlorin heterodimers
    Xiaoxu Kai
    Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P R China
    Chem Commun (Camb) 48:4302-4. 2012

Collaborators

  • Qian Peng
  • Jiaxun Jiang
  • Xiaoxu Kai
  • Zhiqiang Feng
  • Baozhen Liu
  • Yong Wang

Detail Information

Publications5

  1. pmc Effects of imidazole deprotonation on vibrational spectra of high-spin iron(II) porphyrinates
    Chuanjiang Hu
    Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P R China
    Inorg Chem 52:3170-7. 2013
    ....
  2. doi request reprint Chiral recognition of amino acid esters by a novel oxalic amide-linked bisporphyrin
    Jiaxun Jiang
    Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China
    Dalton Trans 42:7651-9. 2013
    ..The chiral recognition mechanism has been further investigated by UV-Vis spectra, (1)H NMR and DFT/TDDFT calculations...
  3. pmc Nuclear resonance vibrational spectra of five-coordinate imidazole-ligated iron(II) porphyrinates
    Chuanjiang Hu
    Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China
    Inorg Chem 51:1359-70. 2012
    ..Our study suggests that the Fe motions are coupled with the porphyrin core and peripheral groups motions. Both peripheral groups and their conformations have significant influence on the vibrational spectra (position and shape)...
  4. pmc Electronic configuration of five-coordinate high-spin pyrazole-ligated iron(II) porphyrinates
    Chuanjiang Hu
    Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China
    Inorg Chem 49:10984-91. 2010
    ..Both the structures and the Mössbauer spectra suggest pyrazole-ligated five-coordinate iron(II) porphyrinates have the same electronic configuration as imidazole-ligated species...
  5. doi request reprint Facile one-pot synthesis of unprecedented β,β'-linked porphyrin-chlorin heterodimers
    Xiaoxu Kai
    Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P R China
    Chem Commun (Camb) 48:4302-4. 2012
    ..These species have been characterized by mass spectroscopy, (1)H NMR, X-ray crystallography, cyclic voltammetry, UV-vis and fluorescence spectroscopy...