Interest in molecular magnets continues to grow, offering a link between the atomicand nanoscale properties. The classical Heisenberg model has been effective inmodelling exchange interactions in such systems. In this, the magnetizationand susceptibility are calculated through the partition function, where theHamiltonian contains both Zeeman and exchange energy. For an ensemble ofN spins, this requiresintegrals in 2N dimensions. For two, three and four spin nearest-neighbour chains these integralsreduce to sums of known functions. For the case of the three and four spin chains,the sums are equivalent to results of Joyce. Expanding these sums, the effect ofthe exchange on the linear susceptibility appears as Langevin functions withexchange term arguments. These expressions are generalized here to describe anN spin nearest-neighbour chain, where the exchange between each pair of nearest neighboursis different and arbitrary. For a common exchange constant, this reduces to the result ofFisher. The high-temperature expansion of the Langevin functions for the differentexchange constants leads to agreement with the appropriate high-temperature quantumformula of Schmidt et al, when the spin number is large. Simulations are presented foropen linear chains of three, four and five spins with up to four different exchangeconstants, illustrating how the exchange constants can be retrieved successfully.
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