Characteristic absorption band split of symmetrically tetra-octyloxy metal phthalocyanines

2015 ◽  
Vol 120 ◽  
pp. 1-7 ◽  
Author(s):  
Fangdi Cong ◽  
Zhen Wei ◽  
Zhiqiang Huang ◽  
Fengyang Yu ◽  
Haixue Liu ◽  
...  
1979 ◽  
Vol 33 (6) ◽  
pp. 578-581
Author(s):  
Norman G. Foster ◽  
Bernice B. Bonner ◽  
Robert W. Higgins

The infrared spectra of six 1-(2-thienyl)-3-thiaalkanes and seven 1-(2-thienyl)-4-thiaalkanes (molecular weights from 186 to 270) were obtained for the 4000 to 400 cm−1 range. These spectra are compared with spectra of other thiophene ring compounds substituted in the 2-position for their characteristic absorption bands. The spectra agree with other spectra as to the major absorption band around 680 cm−1 and the 2-substitution overtone pattern. A method of distinguishing between the two groups of compounds from moderate peaks in the 600 to 500 cm−1 (KBr) region is shown. Interference from the 2-alkylthiophenes and the 1-(2-thienyl)-1-thiaalkanes does not occur.


1992 ◽  
Vol 283 (2) ◽  
pp. 327-331 ◽  
Author(s):  
O Ploux ◽  
A Marquet

The 8-amino-7-oxopelargonate synthase [6-carboxyhexanoyl-CoA:L-alanine carboxyhexanoyltransferase (decarboxylating); EC 2.3.1.47] from Bacillus sphaericus involved in biotin biosynthesis was purified from an Escherichia coli overproducing strain. The purification afforded an electrophoretically homogeneous enzyme with a specific activity of 0.67 unit/mg. The purified enzyme is a monomer of 41 kDa. N-Terminal sequencing of the first 14 amino acid residues showed complete agreement with the predicted sequence from the bioF gene. The pure enzyme showed the characteristic absorption band (425 nm) of pyridoxal 5′-phosphate-dependent enzymes. Furthermore, the holoenzyme was resolved during an affinity step yielding the inactive apoenzyme, which recovered activity and the 425 nm-absorption band on dialysis against pyridoxal 5′-phosphate. Km values for L-alanine and pimeloyl-CoA were respectively 3 mM and 1 microM.


1955 ◽  
Vol 8 (3) ◽  
pp. 355 ◽  
Author(s):  
RL Werner ◽  
KG O'Brien

The infra-red spectra of a series of alkyl and aryl esters of boric acid have been obtained in the region from 1800 to 670 cm-1. These all show a strong characteristic absorption band at 1340 � 10 cm-1 which is assigned to the asymmetrical stretching frequency of the BO3 group. Comparison of the infra-red and Raman spectra of trimethyl borate suggests the assignment of the 728 cm-1 Raman band to the symmetrical stretching mode. The non-coincidence of infra-red and Raman bands indicates a fairly high degree of symmetry with restriction of the rotation of the methyl groups round the B-O link. This contrasts with other data on the behaviour in the vapour where such rotation may occur.


Numerous studies have been made of the absorption spectrum of the products of ultra-violet radiation of ergosterol (1). These studies have shown that such radiation causes a decrease and final disappearance of the characteristic absorption band of ergosterol (maximum 280 m μ). Several workers have reported the simultaneous formation of a new absorption band (maximum 240), and have attributed this band to vitamin D. Our own observations, however, have shown (2) that the first effect of ultra-violet radiation on ergosterol, and we have suggested that this is due to the formation of a new substance with an absorption maximum at 280, and that this substance is vitamin D (3). It has also shown that the product having maximum absorption at 240 has no detectable antirachitic activity (4). We have compared the antirachitic activity of irradiated ergosterol solutions with their absorption spectra, both before and after removal of unchanged ergosterol, and have obtained evidence pointing to the successive formation of three substances (or mixtures of substances). Of these, the first has maximum absorption at 280, and is, we believe, vitamin D; the second shows maximum absorption at 240, and has no antirachitic action; the third is similarly inactive, and shows no intense absorption. We propose to refer to these substances as A, B, and C, respectively.


2018 ◽  
Author(s):  
Adrian Cernescu ◽  
Michał Szuwarzyński ◽  
Urszula Kwolek ◽  
Karol Wolski ◽  
Paweł Wydro ◽  
...  

<div><div>Scattering-mode Scanning Near-Field Optical Microscopy (sSNOM) allows one to obtain absorption spectra in the mid-IR region for samples as small as 20 nm in size. This configuration has made it possible to measure FTIR spectra of the protein complement of membranes. (Amenabar 2013) We now show that mid-IR sSNOM has the sensitivity required to measure spectra of phospholipids in individual bilayers in the spectral range 800 cm<sup>-1</sup>–1400 cm<sup>-1</sup>. We have observed the main absorption bands of the dipalmitoylphosphatidylcholine headgroups in this spectral region above noise level. We have also mapped the phosphate absorption band at 1070 cm<sup>-1</sup> simultaneously with the AFM topography. We have shown that we could achieve sufficient contrast to discriminate between single and multiple phospholipid bilayers and other structures, such as liposomes. This work opens the way to further research that uses nano-IR spectroscopy to describe the biochemistry of cell membranes and model systems.</div></div><div></div>


2020 ◽  
Vol 17 (6) ◽  
pp. 488-495
Author(s):  
Hussein Ali Al-Bahrani ◽  
Mohanad Mousa Kareem ◽  
Abdul Amir Kadhum ◽  
Nour A. Alrazzak

Background: The phthalocyanines a series of compounds involves four iso-indole units linked by aza nitrogen atoms bonded with metal atoms that are normally located in the center a phthalocyanines ring. Some of the central metal-phthalocyanines can be excited by ultraviolet light and emit a fluorescence in far-red region. Objective: To synthesize a derivative of phthalocyanines namely 4,4',4' '-tri-(dodecenyl succinic anhydride)- 4' ' '-(5-amino salicylic acid) zinc phthalocyanine with a zinc central metal. Materials and Methods: The reaction of 4- nitro Phthalonitrile and 4- amino Phthalonitrile with ZnCl2 in the presence of dimethyl amino ethanol afforded 4,4',4' '-triamino-4' ' '-nitro zinc phthalocyanine. This product reacted with 5-amino salicylic acid to yield tetra-(5-amino salicylic acid) zinc phthalocyanine. A dodecenyl succinic anhydride was added on the amine group of benzoic rings to afford 4,4',4' '-tri-(dodecenyl succinic anhydride)-4' ' '-(5-amino salicylic acid) zinc phthalocyanine(I), the target compound. Results and Discussion: Compound I is successfully synthesized with a yield of 72% from tetra-(5-amino salicylic acid) zinc phthalocyanine with dodecenyl succinic anhydride. Conclusion: The newly synthesized molecule of 4,4',4' '-tri-(dodecenyl succinic anhydride)-4' ' '-(5-amino salicylic acid) zinc phthalocyanine (I), tetra-(5-amino salicylic acid) zinc phthalocyanine(E) and 4,4',4' '- triamino-4' ' '-nitro zinc phthalocyanine (S). The reaction of 4- nitro Phthalonitrile and 4- amino and the structure of compound I is confirmed and its formation was proven.


1998 ◽  
Vol 495 (2) ◽  
pp. 941-945 ◽  
Author(s):  
T. H. Kerr ◽  
R. E. Hibbins ◽  
S. J. Fossey ◽  
J. R. Miles ◽  
P. J. Sarre

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