eQion

	A	B	C	D	E	F
1			Energy (eV)
2	Sl. No.	Target	Start	End	Reference	DOI Link

3	1	(CH_3)_2CO (acetone)	50	10000	AIP Advances 5 (2015)	https://doi.org/10.1063/1.4931631
4	2	(CH_3)_2SO (dimethyl sulphoxide)	1	2000	Mol. Phys. 113 (2015) 3883-3890	https://doi.org/0.1080/00268976.2015.1075621
5	3	(CH_3CH_2)_2S (diethyl sulphide)	1	2000	Mol. Phys. 113 (2015) 3883-3890	https://doi.org/0.1080/00268976.2015.1075621
6	4	(CH3CH2CH2)_2S (dipropyl sulphide)	1	2000	Mol. Phys. 113 (2015) 3883-3890	https://doi.org/0.1080/00268976.2015.1075621
7	5	1-C_3H_7Cl (1- chloropropane)	12	5000	Int. J. Mass Spectrom. 360 (2014) 39-44	https://doi.org/10.1016/j.ijms.2013.12.019
8	6	1-C_4H_9Cl (1- chlorobutane)	12	5000	Int. J. Mass Spectrom. 360 (2014) 39-44	https://doi.org/10.1016/j.ijms.2013.12.019
9	7	Ag (Silver)	8	2000	Can. J. Phys. 91 (2013) 744-750	https://doi.org/10.1139/cjp-2013-0174
10	8	AlBr_3 (Aluminium bromide)	10.4	5000	Mol. Phys. 116 (2017) 1208-1217	https://doi.org/10.1080/00268976.2017.1416197
11	9	AlCl_3 (Aluminium chloride)	12.01	5000	Mol. Phys. 116 (2017) 1208-1217	https://doi.org/10.1080/00268976.2017.1416197
12	10	AlF_3 (Aluminium fluoride)	15.45	5000	Mol. Phys. 116 (2017) 1208-1217	https://doi.org/10.1080/00268976.2017.1416197
13	11	AlI_3 (Aluminium iodide)	9.1	5000	Mol. Phys. 116 (2017) 1208-1217	https://doi.org/10.1080/00268976.2017.1416197
14	12	Ar_2 (Argon dimer)	18	2000	Mol. Phys. 111 (2013) 3047-3053	https://doi.org/10.1080/00268976.2013.766369
15	13	B (Boron)	9	2000	Chin. J. Phys. 51 (2013) 1172-1183	https://doi.org/10.6122/CJP.51.1172
16	14	BBr_3 (Boron tribromide)	10.51	5000	Mol. Phys. 116 (2017) 1208-1217	https://doi.org/10.1080/00268976.2017.1416197
17	15	BCl_3 (Boron trichloride)	11.6	5000	Mol. Phys. 116 (2017) 1208-1217	https://doi.org/10.1080/00268976.2017.1416197
18	16	Be (Beryllium)	10	2000	Chin. J. Phys. 51 (2013) 1172-1183	https://doi.org/10.6122/CJP.51.1172
19	17	Be_10W (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
20	18	Be_11W (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
21	19	Be_12W (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
22	20	Be_2W (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
23	21	Be_3W (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
24	22	Be_4W (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
25	23	Be_5W (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
26	24	Be_6W (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
27	25	Be_7W (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
28	26	Be_8W (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
29	27	Be_9W (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
30	28	BeW (Beryllium-tungsten clusters)	0.1	10000	Phys. Plasmas 24 (2017) 83514	https://doi.org/10.1063/1.4997611
31	29	BF_3 (Boron trifluoride)	15.7	5000	Mol. Phys. 116 (2017) 1208-1217	https://doi.org/10.1080/00268976.2017.1416197
32	30	BI_3 (Boron triiodide)	9.25	5000	Mol. Phys. 116 (2017) 1208-1217	https://doi.org/10.1080/00268976.2017.1416197
33	31	Br (Bromine)	10	5000	J. Phys. B: At. Mol. Opt. Phys 53 (2020) 145101	https://doi.org/10.1088/1361-6455/ab8e26
34	32	C_10H_22Cl_2N_2O_4Pt (Satraplatin)	12	5000	Mol. Phys. 114 (2016) 3104-3111	https://doi.org/10.1080/00268976.2016.1219408
35	33	C_10H_8 (Naphthalene)	8.14	5000	J. Chem. Phys. 150 (2019) 64313	https://doi.org/10.1063/1.5081841
36	34	C_2 (Dicarbon)	14	2000	Mol. Phys. 111 (2013) 269-275	https://doi.org/10.1080/00268976.2012.718807
37	35	C_2 H_6 S (dimethyl sulphide)	1	2000	Mol. Phys. 113 (2015) 3883-3890	https://doi.org/0.1080/00268976.2015.1075621
38	36	C_2Cl_6 (Hexachloroethane)	12	5000	Int. J. Mass Spectrom. 373 (2014) 34-38	https://doi.org/10.1016/j.ijms.2014.08.003
39	37	C_2H_2Cl_4 (Tetrachloroethane)	12	5000	Int. J. Mass Spectrom. 373 (2014) 34-38	https://doi.org/10.1016/j.ijms.2014.08.003
40	38	C_2H_3Cl_3 (1,1,1-Trichloroethane)	12	5000	Int. J. Mass Spectrom. 373 (2014) 34-38	https://doi.org/10.1016/j.ijms.2014.08.003
41	39	C_2H_4Cl_2 (1,2-dichloroethane)	12	5000	Int. J. Mass Spectrom. 373 (2014) 34-38	https://doi.org/10.1016/j.ijms.2014.08.003
42	40	C_2H_5CHO (Propionaldehyde )	12	2000	J. Chem. Phys 141 (2014) 54303	https://doi.org/10.1063/1.4891472
43	41	C_2H_5Cl (Chloroethane)	12	5000	Int. J. Mass Spectrom. 360 (2014) 39-44	https://doi.org/10.1016/j.ijms.2013.12.019
44	42	C_2H_5CN (Ethyl cyanide )	12	5000	J. Electron Spectrosc. Relat. Phenom. 205 (2015) 74–82	https://doi.org/10.1016/j.elspec.2015.08.013
45	43	C_2H_5COCH_3 (2-Butanone )	12	2000	J. Chem. Phys 141 (2014) 54303	https://doi.org/10.1063/1.4891472
46	44	C_2H_5NO (N-methylformamide)	11	2000	Mol. Phys. 112 (2014) 1201-1209	https://doi.org/10.1080/00268976.2013.839841
47	45	C_2H_8N_2O_3Pt (Nedaplatin)	10	5000	Mol. Phys. 114 (2016) 3104-3111	https://doi.org/10.1080/00268976.2016.1219408
48	46	C_2H-6O (dimethyl ether)	10.025	5000	Int. J. Mass Spectrom. 409 (2016) 45299	https://doi.org/10.1016/j.ijms.2016.09.002
49	47	C_2HCl_5 (Pentachloroethane)	12	5000	Int. J. Mass Spectrom. 373 (2014) 34-38	https://doi.org/10.1016/j.ijms.2014.08.003
50	48	C_3 (Triatomic-carbon)	14	2000	Mol. Phys. 111 (2013) 269-275	https://doi.org/10.1080/00268976.2012.718807
51	49	C_3F_6O (Hexafluoroacetone)	12.051	5000	J. Phys. B: At. Mol. Opt. Phys. 53 (2019) 145101	https://doi.org/10.1088/1361-6455/ab8e26
52	50	C_3F_6O (Hexafluoropropylene oxide)	12.051	5000	J. Phys. B: At. Mol. Opt. Phys 53 (2020) 145101	https://doi.org/10.1088/1361-6455/ab8e26
53	51	C_3H_6 (Cyclopropane )	12	2000	J. Chem. Phys 141 (2014) 54303	https://doi.org/10.1063/1.4891472
54	52	C_3H_6 (Propene)	0.1	5000	J. Appl. Phys. 124 (2018) 34901	https://doi.org/10.1063/1.5032135
55	53	C_3H_7CHO (Butyraldehyde )	12	2000	J. Chem. Phys 141 (2014) 54303	https://doi.org/10.1063/1.4891472
56	54	C_3H_7CN (n-Propyl cyanide )	12	5000	J. Electron Spectrosc. Relat. Phenom. 205 (2015) 74–82	https://doi.org/10.1016/j.elspec.2015.08.013
57	55	C_3H_7COCH_3 (2-Pentanone)	12	2000	J. Chem. Phys 141 (2014) 54303	https://doi.org/10.1063/1.4891472
58	56	C_3H_9N (n-propylamine)	10	2000	Mol. Phys. 112 (2014) 1201-1209	https://doi.org/10.1080/00268976.2013.839841
59	57	C_3HN (cyanoacetylene)	0.5	5000	J. Phys. B: At. Mol. Opt. Phys. 49 (2016)	https://doi.org/10.1088/0953-4075/49/22/225202
60	58	C_4 H_10 S_2 (di-ethyl disulphide )	1	2000	Mol. Phys. 113 (2015) 3883-3890	https://doi.org/0.1080/00268976.2015.1075621
61	59	C_4F_7N (Heptafluorobutyronitrile)	14.32	5000	J. Phys. B: At. Mol. Opt. Phys. 53 (2019) 145101	https://doi.org/10.1088/1361-6455/ab8e26
62	60	C_4F_7N (Heptafluorobutyronitrile)	14.32	5000	J. Phys. B: At. Mol. Opt. Phys 53 (2020) 145101	https://doi.org/10.1088/1361-6455/ab8e26
63	61	C_4F_8O (Octafluorotetrahydrofuran)	12.837	5000	J. Phys. B: At. Mol. Opt. Phys. 53 (2019) 145101	https://doi.org/10.1088/1361-6455/ab8e26
64	62	C_4F_8O (Octafluorotetrahydrofuran)	12.837	5000	J. Phys. B: At. Mol. Opt. Phys 53 (2020) 145101	https://doi.org/10.1088/1361-6455/ab8e26
65	63	C_4H_10O (1-Butanol)	9.99		Int. J. Mass Spectrom. 431 (2018) 37-42	https://doi.org/10.1016/j.ijms.2018.06.001
66	64	C_4H_10O (2-Butanol)	9.88	5000	Int. J. Mass Spectrom. 431 (2018) 37-42	https://doi.org/10.1016/j.ijms.2018.06.001
67	65	C_4H_10O (2-Methyl-1-propanol)	10.02		Int. J. Mass Spectrom. 431 (2018) 37-42	https://doi.org/10.1016/j.ijms.2018.06.001
68	66	C_4H_10O (2-Methyl-2-propanol)	9.9	5000	Int. J. Mass Spectrom. 431 (2018) 37-42	https://doi.org/10.1016/j.ijms.2018.06.001
69	67	C_4H_10O (Diethyl ether)	9.51	5000	Int. J. Mass Spectrom. 409 (2016) 45299	https://doi.org/10.1016/j.ijms.2016.09.002
70	68	C_4H_10OS (di-ethyl sulphoxide)	1	2000	Mol. Phys. 113 (2015) 3883-3890	https://doi.org/0.1080/00268976.2015.1075621
71	69	C_4H_4N_2 (Pyrimidine)	10	2000	Mol. Phys. 112 (2014) 1201-1209	https://doi.org/10.1080/00268976.2013.839841
72	70	C_4H_4S (Thiophene)	9.29	5000	J. Chem. Phys. 150 (2019) 64313	https://doi.org/10.1063/1.5081841
73	71	C_4H_5N (Pyrrole and its isomers)	IP	5000	Eur. Phys. J. D 74 (2020) 198	https://doi.org/10.1140/epjd/e2020-10283-4
74	72	C_4H_5N (Pyrrole)	8.209	5000	J. Chem. Phys. 150 (2019) 64313	https://doi.org/10.1063/1.5081841
75	73	C_4H_6 (1-Butyne)	11	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
76	74	C_4H_6 (1-methylcyclopropene)	10	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
77	75	C_4H_6 (1,2-Butadiene)	10	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
78	76	C_4H_6 (Bicyclo[1.1.0]butane)	9	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
79	77	C_4H_6 (Cyclobutene)	10	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
80	78	C_4H_6 (Methylenecyclopropane)	10	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
81	79	C_4H_9CHO (Pentanaldehyde )	12	2000	J. Chem. Phys 141 (2014) 54303	https://doi.org/10.1063/1.4891472
82	80	C_4H_9CN (n-Butyl cyanide )	12	5000	J. Electron Spectrosc. Relat. Phenom. 205 (2015) 74–82	https://doi.org/10.1016/j.elspec.2015.08.013
83	81	C_5F_10O (Perfluorovaleryl fluoride)	12.016	5000	J. Phys. B: At. Mol. Opt. Phys. 53 (2019) 145101	https://doi.org/10.1088/1361-6455/ab8e26
84	82	C_5F_10O (Perfluorovaleryl fluoride)	12.016	5000	J. Phys. B: At. Mol. Opt. Phys 53 (2020) 145101	https://doi.org/10.1088/1361-6455/ab8e26
85	83	C_5H_12O (1-Pentanol)	10	5000	Int. J. Mass Spectrom. 431 (2018) 37-42	https://doi.org/10.1016/j.ijms.2018.06.001
86	84	C_5H_12O (2-Methylbutan-1-ol)	9.86	5000	Int. J. Mass Spectrom. 431 (2018) 37-42	https://doi.org/10.1016/j.ijms.2018.06.001
87	85	C_5H_12O (2-Pentanol)	9.78		Int. J. Mass Spectrom. 431 (2018) 37-42	https://doi.org/10.1016/j.ijms.2018.06.001
88	86	C_5H_12O (3-Methylbutan-2-ol)	9.88	5000	Int. J. Mass Spectrom. 431 (2018) 37-42	https://doi.org/10.1016/j.ijms.2018.06.001
89	87	C_5H_12O (3-Pentanol)	9.78	5000	Int. J. Mass Spectrom. 431 (2018) 37-42	https://doi.org/10.1016/j.ijms.2018.06.001
90	88	C_5H_5N (Pyridine)	10	2000	Mol. Phys. 112 (2014) 1201-1209	https://doi.org/10.1080/00268976.2013.839841
91	89	C_5H_5N (Pyridine)	9.6	5000	J. Chem. Phys. 150 (2019) 64313	https://doi.org/10.1063/1.5081841
92	90	C_5H_8 ((E)-1,3-pentadiene)	9	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
93	91	C_5H_8 ((Z)-1,3-pentadiene)	9	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
94	92	C_5H_8 (1-pentyne)	11	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
95	93	C_5H_8 (1,2-pentadiene)	10	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
96	94	C_5H_8 (1,4-pentadiene)	10	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
97	95	C_5H_8 (2,3-pentadiene)	10	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
98	96	C_5H_8 (3-methyl-1,2-butadiene)	9	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
99	97	C_5H_8 (Bicyclo[1.1.1]pentane)	10	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756
100	98	C_5H_8 (Bicyclo[2.1.0]pentane)	9	5000	J. Phys. Chem. A 127 (2023) 5414-5423	https://doi.org/10.1021/acs.jpca.3c01756