X-ray Raman scattering: a new in situ probe of molecular structure during nucleation and crystallization from liquid solutions. Issue 43 (28th September 2018)

• Record Type: Journal Article
• Authors: Al-Madhagi, Laila H.; Chang, Sin-Yuen; Balasubramanian, Mahalingam; Kroner, Anna B.; Shotton, Elizabeth J.; Willneff, Elizabeth A.; Mishra, Bhoopesh; Schroeder, Sven L. M.
• Is Part Of: CrystEngComm. Volume 20:Issue 43(2018)
• Page Start: 6871
• Page End: 6884
• Publication Date: 2018-09-28
• Subjects: Crystals -- Periodicals; Crystal growth -- Periodicals; Crystallography -- Periodicals; Cristaux -- Périodiques; Cristaux -- Croissance -- Périodiques; Cristallographie -- Périodiques; 548
• DOI: 10.1039/c8ce00929e
• Languages: English
• ISSNs: 1466-8033

Abstract

Abstract : X-ray Raman scattering (XRS) has been used for in situ probing of solute molecule speciation in solution during cooling crystallization. Abstract : X-ray Raman scattering (XRS) has been used for in situ probing of solute molecule speciation in solution during cooling crystallization. The C and N K-edges of aqueous imidazole were measured as a function of temperature to monitor the transition from the undersaturated state through supersaturation to crystallization. A new jacketed-vessel crystallizer with internal flow was used, which enables thermal control and minimizes radiation damage. We have demonstrated that the C and N K-edges of imidazole are sensitive to changes in local bonding. In line with this, an abrupt change in the N K-edge fine structure indicates the onset of desolvation and crystallization from the supersaturated solution. In contrast, negligible changes are observed in the C and N K-edge spectra acquired during cooling, indicating that the average solvation structure around imidazole molecules does not change significantly while traversing the thermodynamically metastable supersaturated zone. To the best of our knowledge this is the first time X-ray Raman scattering has been used for studying molecular speciation in organic aqueous solutions during crystallization. Time-dependent density functional theory (TD-DFT) calculations of the near-edge spectra were performed using implicit, explicit and combined solvation models to elucidate the likely binding sites of the water molecules. An explicit solvation model with one water molecule coordinating each nitrogen moiety in the imidazole ring accurately reproduces the peak positions and intensities of the XRS spectra of aqueous imidazole solution.