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X‐ray structure study of the light‐induced metastable states of the spin‐crossover compound [Fe(mtz) 6 ](BF 4 ) 2
Author(s) -
Kusz Joachim,
Spiering Hartmut,
Gütlich Philipp
Publication year - 2001
Publication title -
journal of applied crystallography
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.429
H-Index - 162
ISSN - 1600-5767
DOI - 10.1107/s0021889801000462
Subject(s) - spin crossover , metastability , spin transition , chemistry , spin states , crystallography , excited state , crystal structure , crystal (programming language) , irradiation , single crystal , atomic physics , physics , inorganic chemistry , organic chemistry , computer science , nuclear physics , programming language
Iron(II) complexes exhibiting thermal spin‐crossover may be converted from the 1 A 1 low‐spin (LS) state to the 5 T 2 high‐spin (HS) state by irradiation with green light (light‐induced excited spin‐state trapping, LIESST) and from the LS to the HS state by irradiation with red light (reverse LIESST). The lifetime of the metastable LIESST states may be sufficiently long to enable an X‐ray diffraction study. The lattice parameters of a single crystal of [Fe(mtz) 6 ](BF 4 ) 2 (mtz = methyltetrazole) (space group P 2 1 / n ) were measured between 300 and 10 K. While one Fe lattice site ( A ) of the crystal changes from the HS to the LS state near 78 K, the other site ( B ) remains in the LS state. Using the green light (514 nm) of an argon ion laser the crystal was quantitatively converted to the HS state at 10 K. Irradiation of the crystal at 10 K by red light of a laser diode (820 nm) with site A in the LS and site B in the HS state converts site B almost completely to the LS state. The lattice parameters of both metastable states were measured up to 50 K, where they start to decay on a minute timescale. At 10 K, a full data set for evaluation of the crystal structure was recorded. The volume change of the crystal per complex molecule accompanying the spin transition is 31.5 Å 3 at site A and close to zero [−0.21 (14) Å 3 ] at site B .