The scattering function and radius of gyration of an ideal polymer net
work are calculated depending on the strength of the bonds that form t
he crosslinks. Our calculations are based on an exact theorem for the
characteristic function of a polydisperse phantom network that allows
for treating the crosslinks between pairs of randomly selected monomer
s as quenched variables without resorting to replica methods. From thi
s new approach it is found that the scattering function of an ideal ne
twork obeys a master curve which depends on one single parameter x = (
ak)N-2/M, where ak is the product of the persistence length times the
scattering wavevector, N the total number of monomers and M the crossl
inks in the system. By varying the crosslinking potential from infinit
y (hard delta-constraints) to zero (free chain), we have also studied
the crossover of the radius of gyration from the collapsed regime wher
e R(g) similar or equal to O(1) to the extended regime R(g) similar or
equal to O(root N). In the crossover regime the network size R(g) is
found to be proportional to (N/M)(1/4). The latter result can be under
stood in terms of a simple Flory argument.