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Chapter – 1 Preparation and Yield optimization.....<br />

1.6 SPECTRAL DISCUSSION<br />

1.6.1 MASS SPECTRAL STUDY<br />

Mass spectra of the synthesized compounds were recorded on<br />

Shimadzu GC-MS QP-2010 model using direct injection probe technique.<br />

The molecular ion peak was found in agreement with molecular weight of the<br />

respective compound. Characteristic M +2 ion peaks with one-third intensity of<br />

molecular ion peak were observed in case of compounds having chlorine<br />

atom. Fragmentation pattern can be observed to be particular for these<br />

compounds and the characteristic peaks obtained for each compound.<br />

Probable fragmentation pattern for DNJ-102 and DNJ-206 can be discussed<br />

as under.<br />

2-methyl-1-(morpholin-4-ylmethyl) indoline (DNJ-102)<br />

1. The target compound showed characteristic molecular ion peak.<br />

2. C2-C3 and C5-C6 bond cleavage gave characteristic peak at 190 m/e.<br />

[1]<br />

3. C3-N4 and C5-N4 bond cleavage gave characteristic peak at 160 m/e.<br />

[2]<br />

4. N4-C7 bond cleavage gave characteristic peak, which is the BASE<br />

PEAK at 146 m/e. [3]<br />

5. C7-N8 bond cleavage gave two characteristic peaks. One peak at 130<br />

m/e and second peak at 100 m/e , which is the second intense peak in<br />

the spectrum. [4]<br />

6. After cleaved from bond C7-N8, C9-C17 bond cleavage gave<br />

characteristic peak at 118 m/e. [5]<br />

Department of Chemistry, <strong>Saurashtra</strong> <strong>University</strong>, Rajkot-360 005 46

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