178Reaction optimization by parallel kinetic studies with the FLUOstar Omega

James E. Redman, School of Chemistry, Cardiff University, 08/2008
  • Kinetic studies on the metallation of porphyrin
  • Changes in the absorbance spectra monitored with the FLUOstar® Omega
  • Relative reaction rate in twelve different solvents determined in parallel


The yields of chemical reactions may vary considerably with parameters such as solvent, catalyst, temperature and reaction time. A challenge for the chemist is to optimize these parameters to obtain a satisfactory yield at acceptable time and cost. To aid optimization, a number of devices are available that increase the number of reactions that can conveniently be performed in parallel by an individual chemist. 

In situations where reactants and products differ in their molar extinction coefficients the reaction progress can be followed directly by UV-visible spectroscopy. Rather than determining the concentrations of species by physical separation and individual quantitation, a time-series of spectra in which these species vary in their relative proportions can be analysed mathematically accompanied by derivation of kinetic rate constants by least squares fitting.

Devices such as the Radleys carousel reactor allow 12 reactions to be performed simultaneously on one standard hot-plate stirrer. Reaction aliquots sampled as a function of time are therefore readily accommodated in the 12 columns of a 96-well microplate. Monitoring is ideally suited to the BMG LABTECH FLUOstar Omega microplate reader due to its ability to acquire a full UV-visible spectrum of each well in under one second.

In this example, we have monitored the metallation of a porphyrin with Zn2+ (Figure 1) as a function of solvent. The porphyrin starting material and product are both highly coloured and the reaction proceeds with a perceptible but subtle colour change. The absorption spectra of the two species overlap significantly making a global least squares analysis of spectra desirable for quantitative rate comparisons.

Fig. 1: Metallation of tetraphenylporphyrin (TPP) with zinc.

Materials & Methods

  • BMG LABTECH FLUOstar Omega microplate reader Corning Costar flat bottom polypropylene 96-well microplates
  • Tetramethylrhodamine methyl ester (TMRM), Sigma
  • Radleys Carousel 12 Reaction Station, with magnetic stirrer
  • Specfit/32 software (Spectrum Software Associates)

5,10,15,20-Tetraphenylporphyrin (TPP) was prepared by the method of Adler et al. and recrystallized from chloro-form layered with methanol.  Solvents (N, N-dimethyl-formamide (DMF), toluene, chloroform, pyridine, isopro-panol, acetone, N-methyl-2-pyrrolidone (NMP), dichloro-methane, acetonitrile, tetrahydrofuran, ethylacetate and dimethylsulfoxide) were obtained from Acros or Aldrich. Background scans of all wells of a microplate were made on the FLUOstar Omega using the UV/Vis absorbance spectrometer (20 flashes per well, 450–680 nm with 1 nm resolution). TPP (2 mg) was placed with a stirrer bar in each of the 12 tubes of the carousel reactor. Solvent (10 mL) was added to each tube, which was stirred for ~15 minutes to allow dissolution of the porphyrin. Aliquots (50 μL) were removed from each tube and diluted with DMF (200 μL) in columns 1-12 of row A of the microplate, which was immediately scanned. 

Zn(OAc)2.2H2O (obtained from Avocado) portions were weighed (12 × 7 mg), then one portion added in quick succession to each carousel tube to initiate the reaction. After total times of 10, 30, 60, 120, 240, 480 and 1440 minutes, aliquots (50 μL) were withdrawn from each tube, diluted with DMF (200 μL) in a microplate row and scanned immediately. 

The empty plate background was subtracted and the absorbance at 680 nm set to zero for each scan by subtracting a constant offset at all wavelengths. The data were subjected to singular value decomposition using the Specfi t/32 software, followed by kinetic modelling according to the scheme TPP → ZnTPP where both are coloured species with first order kinetics with respect to TPP. The Zn2+ concentration remains approximately constant due to the ten fold excess used, and no significant difference in the relative rates or quality of fi t was observed if the reaction was modelled as TPP + Zn2+ → ZnTPP, with colourless Zn2+ and first order with respect to both TPP and Zn2+.

Results & Discussion

The rate of the metallation reaction of tetraphenyl-porphyrin (TPP) with Zn2+ (Figure 1) might show solvent dependence, due to differing degrees of solvation of the porphyrin and zinc salt and the possibility for bases to assist in porphyrin deprotonation. In preliminary experiments polystyrene microplates were found to be attacked too rapidly by most organic solvents, so we investigated the possibility of using flat bottom polypropylene storage plates as an alternative to costly and fragile quartz. At the visible wavelengths of interest, these plates proved to be sufficiently transparent, although it was found necessary to collect a background scan of each well of the empty plate due to well-to-well variation.

Twelve common laboratory solvents spanning a range of polarity and chemical properties were chosen for comparison. Starting material and product were both found to dissolve adequately in DMF. The reaction progress could be qualitatively assessed by visual inspection of spectra (Figure 2 and 3) using the MARS evaluation software, which revealed most rapid reaction in the halogenated solvents dichloromethane and chloroform and little change in N-methyl-2-pyrrolidone (NMP).

Isopropanol and acetonitrile reactions gave lower maximum OD values than the other samples which can be attributed to poor solubility of the TPP starting material in these solvents. For DMSO a black precipitate was apparent in the sampled reaction aliquot, possible evidence of a side reaction.

Fig. 2: Changes in visible spectrum accompanying zinc metallation of TPP in chloroform. Arrows indicate the evolution of the absorption bands with time.Fig. 3: Changes in visible spectrum accompanying zinc metallation of TPP in NMP.To quantify the relative reaction rates in the different solvents, spectra were analysed using the Specfit/32 software. Spectra were subjected to singular value decomposition and globally fitted to a kinetic model in which the only coloured species were TPP and ZnTPP.

The reaction was assumed to be the first order with respect to TPP. There was no evidence from the factor analysis of more than two coloured species, and we were unable to observe the presence of an intermediate that had been suggested in the literature. Acceptable fits to the model were obtained for all solvents (estimated errors <20%), with the exceptions of acetonitrile, isopropanol and DMSO. The relative rates deduced from this analysis are given in Table 1.

Acetonitrile and isopropanol are excluded due to insolubility of the TPP starting material, and the value for DMSO should only be taken as approximate.

Table 1: Rates of reaction of tetraphenylporphyrin with Zn(OAc)2. 2H2O in different solvents, relative to the rate in N-methyl-2-pyrrolidone (NMP).


Solvent Relative initial rate Solvent Relative initial rate
Toluene 10 Dichloromethane 300
Chloroform 100 Tetrahydrofuran 30
Pyridine 2 Ethylacetate 30
Acetone 50 Dimethylsulfoxide ~1


The metallation reaction is fastest in the two halogenated solvents, dichloromethane and chloroform. The rates in the highly polar solvents NMP, DMF and DMSO are amongst the slowest. The basic and aromatic solvent pyridine was less effective than non-basic toluene and two orders of magnitude slower than dichloromethane.


A carousel reactor could be used in conjunction with the FLUOstar Omega to conveniently monitor the kinetics of twelve reactions in parallel. Polypropylene microplates were found to be compatible with measurement of visible spectra of organic solutions, and sampling and scanning of the twelve reactions could be achieved in three minutes.

The ability of the FLUOstar to collect complete spectra enabled the use of singular value decomposition and global least squares fitting to analyse reaction kinetics.

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