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Title: Incorporation of phthalocyanines by cationic and anionic clays via ion exchange and direct synthesis

Journal Article · · Chemistry of Materials; (United States)
DOI:https://doi.org/10.1021/cm00028a013· OSTI ID:6299373
; ;  [1];  [2]
  1. Argonne National Laboratory, IL (United States)
  2. CalTech, Pasadena, CA (United States)

Phthalocyanines (Pc) and metallophthalocyanines were incorporated into the galleries of anionic and cationic clays via ion exchange and in situ crystallization of the synthetic clay layers. Intercalation compounds between the layered magnesium silicate clay hectorite and cationic phthalocyanines were directly prepared by refluxing for 2 days aqueous solutions of silica sol, magnesium hydroxide, lithium flouride, and either alcian blue dyes (Cu(II)Pc) or 15-crown-5 tetra-substituted phthalocyanine (15C5Pc). The CuPc dyes are tetrapositively charged through peripheral quaternary ammonium groups, whereas the 15C5Pc is electrically neutral. Anionic clays prepared by hydrolysis of mixed solutions of aluminum nitrate, magnesium nitrate, and copper(II) phthalocyaninetetrasulfonic acid, tetrasodium salt (CuPcTs) in sodium hydroxide resulted in crystallization of an intercalation compound between a layered double hydroxide (LDH) and this anionic Pc. The material prepared by ion exchange of CuPcTs into a wet, freshly prepared LDH was superior in crystallinity. The phthalocyanines are oriented parallel to cationic hectorite clay layers (gallery heights 4.5-6.5[angstrom]) and perpendicular to anionic layered double hydroxide clay layers (gallery height 18,2[angstrom]) in correlation with their hosts' respective layer charge densities. 32 refs., 4 figs., 2 tabs.

DOE Contract Number:
W-31-109-ENG-38
OSTI ID:
6299373
Journal Information:
Chemistry of Materials; (United States), Vol. 5:4; ISSN 0897-4756
Country of Publication:
United States
Language:
English