TY - JOUR
T1 - Topochemical solid state photodimerization of non-ideally oriented monomers
T2 - 7-chlorocoumarin and 7-methoxycoumarin
AU - Gnanaguru, K.
AU - Ramasubbu, N.
AU - Venkatesan, K.
AU - Ramamurthy, V.
N1 - Funding Information:
We gratefully acknowledge financial support from the University Grants Commission, Government of India,
PY - 1984/12
Y1 - 1984/12
N2 - Photodimerizations of 7-chlorocoumarin and 7-methoxycoumarin in the solid state were studied; syn head-to-head and syn head-to-tail dimers are the respective products of irradiation in the solid state. X-ray crystal structure analyses of 7-chlorocoumarin and 7-methoxycoumarin reveal unusual features. 7-Chlorocoumarin is arranged in a β-type packing, the centre-to-centre distance between the reactive double bonds being 4.454 Å, which lies outside the limit accepted at present of 3.5 - 4.2 Å. In contrast, the reactive double bonds of 7-methoxycoumarin are rotated by about 65° with respect to each other with the centre-to-centre distance between the double bonds being 3.83 Å. In spite of these unfavourable arrangements photodimerization of these two coumarins in the solid state occurs through a topochemical process with large dimer yields.
AB - Photodimerizations of 7-chlorocoumarin and 7-methoxycoumarin in the solid state were studied; syn head-to-head and syn head-to-tail dimers are the respective products of irradiation in the solid state. X-ray crystal structure analyses of 7-chlorocoumarin and 7-methoxycoumarin reveal unusual features. 7-Chlorocoumarin is arranged in a β-type packing, the centre-to-centre distance between the reactive double bonds being 4.454 Å, which lies outside the limit accepted at present of 3.5 - 4.2 Å. In contrast, the reactive double bonds of 7-methoxycoumarin are rotated by about 65° with respect to each other with the centre-to-centre distance between the double bonds being 3.83 Å. In spite of these unfavourable arrangements photodimerization of these two coumarins in the solid state occurs through a topochemical process with large dimer yields.
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U2 - 10.1016/0047-2670(84)80051-9
DO - 10.1016/0047-2670(84)80051-9
M3 - Article
AN - SCOPUS:0003144337
SN - 0047-2670
VL - 27
SP - 355
EP - 362
JO - Journal of Photochemistry
JF - Journal of Photochemistry
IS - 3
ER -