Page 253 - Tunable Lasers Handbook

N Emission data obtained willi solvent listed in first place. For further alternative, solvenls, see Rfs. 3 and 4. Most of the inforinution given in this table has been
.II
adapted from KODAK Laser Dy& courtesy of Eastman Kodak Coiiipaiiy ant1 originally puhlished in D.yc Lnser Princip/es.h
“These are approximate values since the tuning range depends oil solvent, pump source, and resonator charact,erislics.
hThird Harmonic froin Nd:YAG at 355 nm.
“Second Hamionic from Nd:YAG at 532 nm.
References
I. C. H. Chen, J. L. Fox, F J. Duane, and J. J. Ehrlich, Appl. Opt. 27,443 (1088).
2. W. E. Davenport, J. .T. Ehrlich, and S. E. Neister, in Proctwlings of’ the /titww/iord Cnr@crrcc or), La.w ‘89 (D. G. Hurris and T. M. Shay, Eds.), pp,
4084.14, STS Press, McLcan, VA. (1990).
3. K. H. Drexhage, in Dye Losers (E P. Sch,%er, Ed.), pp. 155-200, Springer-Verlag, Berlin, 1990.
4. M. Maeda, La.sev Dgcs, Academic, New York, 1984.
5. R. R. Birge, KODAK k~wr Dyes, Kodnk Publication JJ-169, Eastman Koduk Company, Rochester, NY, (1987).
6. E J. Duaite and L. W. Hillman, “Dyc, Lirscv. friwiph’’> Academic, New York, (I Y90).
Abbreviations: DASBTI, 2-(p-di1nethylaniirlost1yl)-ben~otlii~zolyletliyl iodide; DaQTeC, 1 ,I ’-diethyl- I3-acetoxy-2,2’-quinotetncarh~y~nine iodide; DCM, 4-
dicylmo1nelliylene-2-me1l~yl-6-l,-dime1 hylnininostryl-4H-pyr~in; DCCI, I, I ’-diethyl-2,4’-carbocyaniiie iodide; =DCI, I, 1 ’-diethyl-2,4’-carbocyanhie iodide;
DCCI”‘, I, I ’-diethyl-2, 2’-carbocyilnine iodide; =DDI, DOCI, 3,3’-diethyl oxacarbocyanine iodide; DODCI, 3,3’-diethyI oxadicarbocyanine iodide; DOTCI, 3,3’-
diethyl oxatricarbocyanine iodide; DQOCI, 1,3’-diethyl-4,2’quinolyoxacarbocyilnilie iodide; HICI, 1,1’3.3,3’,3 ’-liexamethylindocarl~ocy~~i~ne iodide; HITCI,
1 ,I ‘3,3,3’,3’-hexuinethylii~dotricarbocynliine iodide; MNA, 2-niethyl-4-nitroaniline.
*Cryplocyanine I, 1 ’-Diethyl-4,4’-carbocynniiie iodide; DTDCI, 3,3’-Diethyl thisdicarbocyanine iodide; DQTCI, I ,3’-Diethyl-4,2’-quinolthiacurbocyaine iodide.