1 00:00:00,250 --> 00:00:08,097 Some published desktop labels remain in Spanish; this English narration guides the controls. This is the real 2 00:00:08,097 --> 00:00:14,560 DiffAtOnce Legacy interface for Windows in a demonstration environment. The walkthrough uses a prepared 3 00:00:14,560 --> 00:00:19,176 synthetic project. It does not show an experimental Bruker import. 4 00:00:20,176 --> 00:00:27,412 Opening the project retains three ramps and sixty-nine synthetic spectra. Check the detected acquisitions before 5 00:00:27,412 --> 00:00:32,718 choosing one. Keep the conditions of each series separate during analysis. 6 00:00:33,718 --> 00:00:41,718 The selector lists three ramps with twenty-three spectra each. Choose the acquisition you want to analyze and 7 00:00:41,718 --> 00:00:46,895 review its metadata. Experiment numbering cannot replace the physical acquisition parameters. 8 00:00:47,895 --> 00:00:55,181 Use series activates the chosen ramp and displays its pulse program, timings and temperature. Review those 9 00:00:55,181 --> 00:01:02,012 original values before calculating. This example is not a new experimental calibration of the probe. 10 00:01:03,012 --> 00:01:11,287 A double click near the peak selects its original local maximum. The marker is close to seven point two six 11 00:01:11,287 --> 00:01:15,839 parts per million. Tracking information identifies the monitored position and spectrum. 12 00:01:16,839 --> 00:01:24,667 The catalogue shows molecular references, but no identity has been assigned here. Context needed to check 13 00:01:24,667 --> 00:01:31,516 compatibility is still missing. Review nucleus, medium, companion signals and sources before labeling a 14 00:01:31,516 --> 00:01:32,006 molecule. 15 00:01:33,006 --> 00:01:39,681 Rectangle zoom enlarges the chosen region while retaining the tracked resonance. Changing the view does not 16 00:01:39,681 --> 00:01:45,523 modify intensities. Continue with the diffusion fit or save a copy of the project.