Table 3. Hyperpolarizability Values for DHAs and VHFs (Electron-Donating Groups).

no.	substituents	DHA	VHF	no.	substituents	DHA	VHF
1	8a-PH2	1.40	11.09	31	8a-CH2NH2	1.60	9.48
2	8-PH2	1.37	10.71	32	8-CH2NH2	1.16	8.54
3	7-PH2	0.70	11.37	33	7-CH2NH2	1.38	13.80
4	6-PH2	2.17	11.96	34	6-CH2NH2	3.36	13.53
5	5-PH2	2.08	12.40	35	5-CH2NH2	1.18	13.81
6	4-PH2	1.83	12.25	36	4-CH2NH2	0.73	11.10
7	8a-OMe	0.99	10.05	37	8a-CH2F	1.54	9.26
8	8-OMe	2.65	4.44	38	8-CH2F	1.27	11.07
9	7-OMe	2.74	13.40	39	7-CH2F	1.39	13.61
10	6-OMe	9.09	16.30	40	6-CH2F	1.32	14.41
11	5-OMe	4.26	15.59	41	5-CH2F	0.84	14.80
12	4-OMe	2.49	15.53	42	4-CH2F	1.35	11.94
13	8a-NHMe	1.42	11.04	43	8a-CH2Cl	1.31	12.53
14	8-NHMe	4.91	13.01	44	8-CH2Cl	1.20	10.65
15	7-NHMe	3.32	18.19	45	7-CH2Cl	0.53	14.56
16	6-NHMe	14.10	15.02	46	6-CH2Cl	0.41	12.64
17	5-NHMe	5.45	13.20	47	5-CH2Cl	0.55	16.01
18	4-NHMe	4.26	7.74	48	4-CH2Cl	0.98	11.67
19	8a-NMe2	1.53	4.28	49	8a-CH2Br	1.12	12.01
20	8-NMe2	4.17	6.08	50	8-CH2Br	1.09	9.52
21	7-NMe2	4.08	16.47	51	7-CH2Br	1.20	13.56
22	6-NMe2	14.75	19.48	52	6-CH2Br	2.99	12.00
23	5-NMe2	6.99	18.26	53	5-CH2Br	2.46	15.76
24	4-NMe2	3.74	19.48	54	4-CH2Br	2.64	11.86
25	8a-CH2OH	1.68	7.40	28	6-CH2OH	1.71	15.91
26	8-CH2OH	1.54	10.56	29	5-CH2OH	2.18	13.81
27	7-CH2OH	2.24	12.85	30	4-CH2OH	1.63	11.64